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Mansueto Ventures is home to two of the most iconic and vibrant brands in business publishing: Inc. and Fast Company. Every day, the content, awards, and events produced help entrepreneurs and innovators succeed by providing useful insights, sparking essential conversations, and offering much-needed inspiration.

Inc. is the voice of the American entrepreneur, inspiring and documenting the risk-takers and ultra-driven go-getters who represent the most dynamic force in the American economy.
Fast Company is the world’s leading business media brand, focusing on innovation in technology, leadership, and design to inspire readers to shape the future of business.

","New York, NY","coloredLogo","logoAttachment","thumbnail","thumbnailAttachment","hexCode","#080D0C","headline","Publisher of Inc. and Fast Company, empowering innovators and entrepreneurs.","/companies/mansueto-ventures-careers","hasJobSubmission","isSavedJob","similarJobs",[507,517,527,539,548],{"_426":425,"_430":508,"_449":450,"_441":509,"_240":510,"_437":511,"_424":425,"_111":433,"_428":191,"_429":191,"_451":450,"_439":440,"_422":512,"_452":513,"_427":118,"_473":514,"_457":515,"_475":433,"_476":440,"_478":516,"_480":481,"_482":483},["D",1769680800000],"Catalent Pharma Solutions","Lead Specialist, Client QA\nPosition Summary

Work Schedule: Monday – Friday, 8am – 5pm.

100% on-site

Catalent is a leading global CDMO partnering with pharma and biotech innovators to accelerate development and delivery of life-changing therapies. Our FDA-licensed, state-of-the-art CGMP gene therapy campus in Harmans, MD—just minutes from BWI Airport—features EMA and FDA-approved manufacturing suites, fill/finish capabilities, labs, and warehousing to support Phase 3 through commercial production of advanced therapies, including AAV and other viral vector-based products.

The Lead Specialist, QA is responsible for providing QA lead support and oversight of Client Projects from start to finish for GMP Manufacturing of master/working cell banks, biological bulk drug substance and finished drug product. You’ll play a key role in ensuring the quality and compliance of cutting-edge gene therapy products. Acting as the dedicated Client QA Representative, you’ll oversee projects from start to finish—partnering with cross-functional teams in Manufacturing, Process Development, Technology Transfer, and Quality Control. Your work will include reviewing and tracking critical GMP documentation such as technology transfer records, specifications, master batch records, and investigations, all supporting the release of life-changing therapies. This is an opportunity to make a direct impact on patient health while collaborating in a dynamic, growth-driven environment.

The Role

Provide dedicated QA support for client projects and client interactions, serving as the primary QA contact throughout the project lifecycle.

Provides quality oversight of GMP operations for the manufacture of master/working cell banks, bulk drug substance and/or final drug product

Support clinical and commercial QA activities from process development through non-clinical and commercial production.

Track and present key quality metrics for client projects, including batch release timelines and deviation trends.

Collaborate with clients during initial and subsequent manufacturing campaigns to ensure compliance and quality standards.

Review and approve master batch records during technology transfer for client processes.

Supports GMP departments in reviewing and approving deviations and failure investigations, including root cause analysis, evaluating product/facility impacts, and evaluating effective corrective and preventive actions (CAPAs)

Perform risk assessments and mitigation strategies using tools such as FMEA.

Maintain and update systems and databases for tracking manufacturing and quality activities.

Support audits and inspections by regulatory agencies and clients and assist with internal GMP audits.

Other duties as assigned.

The Candidate

Masters’ degree in a Scientific, Engineering or Biotech field with a minimum of 4 years’ experience in Quality Assurance/Quality Control within biologics, biopharmaceuticals, or a regulated industry OR

Bachelor’s degree in a Scientific, Engineering or Biotech field with a minimum of 6 years’ experience in Quality Assurance/Quality Control within biologics, biopharmaceuticals, or a regulated industry.

Strong knowledge base with Good Manufacturing Practices (GMPs), 21 CFR Parts 210, 211, biological regulations per 21 CFR Parts 600s, ICH Guidelines and EU GMPs.

Knowledgeable and/or exposure to biological manufacturing processes including microbial and cell culture cell banking, fermentation/cell culture, purification and fill/finish.

Familiarity with electronic systems, including developing and producing reports using Microsoft products. LIMS, Master Control and Trackwise knowledge preferred.

Creative individual with strong analytical, troubleshooting, and decision-making skills to resolve complex issues effectively.

Ability to quickly learn new and novel manufacturing processes supporting new clients

Proven ability to work independently and in cross-functional teams, delivering high-quality results in a fast-paced, deadline-driven environment while meeting client and regulatory requirements.

The anticipated salary range for this position in Maryland is $120,000 to $150,000 plus an annual bonus, when eligible. The final salary offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Catalent is a multi-state employer, and this salary range may not reflect positions that work in other states.

Why you should Join Catalent

Potential for career growth within an expanding team.

Defined career path and annual performance review & feedback process.

Cross-functional exposure to other areas within the organization.

Medical, Dental, Vision, and 401K are all offered from day one of employment.

152 hours of PTO and 8 paid holidays.

Opportunity to work on Continuous Improvement Processes

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.

Catalent is an Equal Opportunity Employer, including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.

California Job Seekers can find our California Job Applicant Notice here.

#J-18808-Ljbffr\n","Lead Specialist, Client QA\nPosition Summary

Work Schedule: Monday – Friday, 8am – 5pm.

100% on-site

Catalent is a leadin...",["B","2342964912"],"Work at Catalent Pharma Solutions","8 days ago","/jobs/2342964912-lead-specialist-client-qa","/jobs?keyword=Catalent+Pharma+Solutions",{"_426":425,"_430":518,"_449":450,"_441":519,"_240":520,"_437":521,"_424":425,"_111":433,"_428":191,"_429":191,"_451":450,"_439":440,"_422":522,"_452":523,"_427":118,"_473":524,"_457":525,"_475":433,"_476":440,"_478":526,"_480":481,"_482":483},["D",1770051600000],"Maryland Staffing","Lead Specialist, Client QA

Position Summary: Work Schedule: Monday Friday, 8am 5pm. 100% on-site\nCatalent is a leading global CDMO partnering with pharma and biotech innovators to accelerate development and delivery of life-changing therapies. Our FDA-licensed, state-of-the-art CGMP gene therapy campus in Harmans, MDjust minutes from BWI Airportfeatures EMA and FDA-approved manufacturing suites, fill/finish capabilities, labs, and warehousing to support Phase 3 through commercial production of advanced therapies, including AAV and other viral vector-based products. The Lead Specialist, QA is responsible for providing QA lead support and oversight of Client Projects from start to finish for GMP Manufacturing of master/working cell banks, biological bulk drug substance and finished drug product. You'll play a key role in ensuring the quality and compliance of cutting-edge gene therapy products. Acting as the dedicated Client QA Representative, you'll oversee projects from start to finishpartnering with cross-functional teams in Manufacturing, Process Development, Technology Transfer, and Quality Control. Your work will include reviewing and tracking critical GMP documentation such as technology transfer records, specifications, master batch records, and investigations, all supporting the release of life-changing therapies. This is an opportunity to make a direct impact on patient health while collaborating in a dynamic, growth-driven environment.\nThe Role

Provide dedicated QA support for client projects and client interactions, serving as the primary QA contact throughout the project lifecycle.\nProvides quality oversight of GMP operations for the manufacture of master/working cell banks, bulk drug substance and/or final drug product.\nSupport clinical and commercial QA activities from process development through non-clinical and commercial production.\nTrack and present key quality metrics for client projects, including batch release timelines and deviation trends.\nCollaborate with clients during initial and subsequent manufacturing campaigns to ensure compliance and quality standards.\nReview and approve master batch records during technology transfer for client processes.\nSupport GMP departments in reviewing and approving deviations and failure investigations, including root cause analysis, evaluating product/facility impacts, and evaluating effective corrective and preventive actions (CAPAs)\nPerform risk assessments and mitigation strategies using tools such as FMEA.\nMaintain and update systems and databases for tracking manufacturing and quality activities.\nSupport audits and inspections by regulatory agencies and clients and assist with internal GMP audits.\nOther duties as assigned.\nThe Candidate

Masters' degree in a Scientific, Engineering or Biotech field with a minimum of 4 years' experience in Quality Assurance/Quality Control within biologics, biopharmaceuticals, or a regulated industry OR Bachelor's degree in a Scientific, Engineering or Biotech field with a minimum of 6 years' experience in Quality Assurance/Quality Control within biologics, biopharmaceuticals, or a regulated industry.\nStrong knowledge base with Good Manufacturing Practices (GMPs), 21 CFR Parts 210, 211, biological regulations per 21 CFR Parts 600s, ICH Guidelines and EU GMPs.\nKnowledgeable and/or exposure to biological manufacturing processes including microbial and cell culture cell banking, fermentation/cell culture, purification and fill/finish.\nFamiliarity with electronic systems, including developing and producing reports using Microsoft products. LIMS, Master Control and Trackwise knowledge preferred.\nCreative individual with strong analytical, troubleshooting, and decision-making skills to resolve complex issues effectively.\nAbility to quickly learn new and novel manufacturing processes supporting new clients.\nProven ability to work independently and in cross-functional teams, delivering high-quality results in a fast-paced, deadline-driven environment while meeting client and regulatory requirements.\nThe anticipated salary range for this position in Maryland is $120,000 to $150,000 plus an annual bonus, when eligible. The final salary offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc.\nCatalent is a multi-state employer, and this salary range may not reflect positions that work in other states.\nWhy You Should Join Catalent

Potential for career growth within an expanding team.\nDefined career path and annual performance review & feedback process.\nCross-functional exposure to other areas within the organization.\nMedical, Dental, Vision, and 401K are all offered from day one of employment.\n152 hours of PTO and 8 paid holidays.\nOpportunity to work on Continuous Improvement Processes\nCatalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world.\nCatalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.\n","Lead Specialist, Client QA

Position Summary: Work Schedule: Monday Friday, 8am 5pm. 100% on-site\nCatalent is a leading global CDMO partner...",["B","2408878790"],"Work at Maryland Staffing","4 days ago","/jobs/2408878790-lead-specialist-client-qa","/jobs?keyword=Maryland+Staffing",{"_426":425,"_430":528,"_449":450,"_441":529,"_240":530,"_437":531,"_424":425,"_111":532,"_428":191,"_429":191,"_451":450,"_439":440,"_422":533,"_452":534,"_427":118,"_473":535,"_457":536,"_475":532,"_476":440,"_478":537,"_480":481,"_482":538},["D",1769288400000],"Catalent","Position Summary\nCatalent is a leading global CDMO partnering with pharma and biotech innovators to accelerate development and delivery of life-changing therapies. Our FDA-licensed, state-of-the-art CGMP gene therapy campus in Harmans, MD—just minutes from BWI Airport—features EMA and FDA-approved manufacturing suites, fill/finish capabilities, labs, and warehousing to support Phase 3 through commercial production of advanced therapies, including AAV and other viral vector-based products.

Work Schedule:

Monday – Friday, 8am – 5pm.

Work Location:

100% on-site.

The Role

Draft, review, process, and manage supplier, service, and operational contracts, including tracking terms, renewals, pricing, and performance obligations in compliance with company and legal requirements.

Coordinate with Procurement, Legal, Quality, and other stakeholders, maintain organized contract records, and support audits by providing required documentation and compliance evidence.

Serve as the primary point of contact for facility, equipment, and service maintenance, including scheduling preventive maintenance and coordinating vendor service visits in compliance with GMP and validated system requirements.

Maintain equipment calibration, qualification, and maintenance records, track contractor performance, and support facility projects, equipment installations, and vendor onboarding activities.

Process purchase orders, invoices, vendor payments, and expense reports in accordance with finance procedures while maintaining accurate financial records.

Support budgeting, cost tracking, reconciliations, and spend monitoring for maintenance and contract-related expenses, highlighting variances as needed.

Partner with Procurement and Finance on cost control, vendor pricing updates, and audit support, including internal and external audits.

Ensure administrative processes comply with GMP/GDP, SOPs, internal audits, and regulatory requirements, including preparing documentation for regulatory inspections.

Maintain current vendor qualification documentation and protect the confidentiality of sensitive contract and financial information.

Other duties as assigned.

The Candidate

Bachelor’s degree in Business Administration, Finance, Supply Chain, or a related field.

Minimum of 4 years of experience managing vendors or contractors required; experience supporting large facilities is preferred.

Strong understanding of procurement, contracts administration, finance processes, and maintenance coordination required; experience in pharmaceutical, biotech, healthcare, or other regulated industries preferred.

Proficient in ERP systems and MS Office (Excel, Word, PowerPoint), with strong administrative, documentation management, and organizational skills.

Excellent communication, collaboration, and multitasking abilities, with a proactive approach to problem-solving and prioritization.

High attention to detail and accuracy, supported by analytical thinking, financial literacy, and a strong compliance mindset.

Demonstrated professionalism, confidentiality, and effective vendor management when working with internal stakeholders, auditors, contractors, and suppliers.

Compensation and Benefits\nThe anticipated salary range for this position in Maryland is $82,000 to $95,000 plus an annual bonus, when eligible. The final salary offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Catalent is a multi-state employer, and this salary range may not reflect positions that work in other states.

Why You Should Join Catalent

Potential for career growth within an expanding team.

Defined career path and annual performance review & feedback process.

Cross-functional exposure to other areas within the organization.

Medical, Dental, Vision, and 401K are all offered from day one of employment.

152 hours of PTO and 8 paid holidays.

Opportunity to work on Continuous Improvement Processes.

Catalent offers rewarding opportunities to further your career. Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

Equal Opportunity Employer statements and accommodations: Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.

California Job Seekers can find our California Job Applicant Notice HERE.

#J-18808-Ljbffr\n","Position Summary\nCatalent is a leading global CDMO partnering with pharma and biotech innovators to accelerate development and delivery of life-cha...","Contract Management Specialist",["B","2273688951"],"Work at Catalent","13 days ago","/jobs/2273688951-contract-management-specialist","/jobs?keyword=Catalent","/jobs?keyword=Contract+Management+Specialist",{"_426":425,"_430":540,"_449":450,"_441":509,"_240":541,"_437":542,"_424":425,"_111":543,"_428":191,"_429":191,"_451":450,"_439":440,"_422":544,"_452":513,"_427":115,"_473":545,"_457":546,"_475":543,"_476":440,"_478":516,"_480":481,"_482":547},["D",1769767200000],"Director, Human Resources

Position Summary\n100% onsite

Catalent is a leading global CDMO partnering with pharma and biotech innovators to accelerate development and delivery of life-changing therapies. Our FDA-licensed, state-of-the-art CGMP gene therapy campus in Harmans, MD—just minutes from BWI Airport—features EMA and FDA-approved manufacturing suites, fill/finish capabilities, labs, and warehousing to support Phase 3 through commercial production of advanced therapies, including AAV and other viral vector-based products.\nWe are seeking a Director of Human Resources who will have full responsibility for the Maryland Gene Therapy business which is inclusive of two (2) manufacturing sites, one (1) training center and administrative office, and one (1) 3PL off-site warehouse. This position will drive strategic and tactical HR roles for the site. This includes being a full member of the Site Leadership Team and being a strategic business partner to the General Manager and the various functional leaders. This senior level position reports to the Biologics Segment Head of HR and will be leading the site HR team.\nThe Role\nHR Strategy and Planning: Develop and implement the site HR strategy aligned with the organization's objectives. Collaborate with senior management to identify and address HR needs and challenges. Provide guidance and support in workforce planning and employee retention efforts.

Employee Relations: Serve as a trusted advisor to employees and management, providing guidance on HR policies, procedures, and best practices. Manage employee relations matters, including conflict resolution, disciplinary actions, and performance management. Ensure compliance with labor laws, regulations, and company policies.

Talent Assessment, Management and Development: Responsible and accountable for assessment of site people leaders. Oversee the talent management process, including performance evaluations, career development, and succession planning. Collaborate with managers to identify training and development needs and identify the appropriate programs.

Compensation and Benefits: Partner with the compensation team to develop and administer local compensation and benefits programs. Ensure compliance with local legislation and market practices. Provide guidance on rewards and recognition initiatives.

Employee Engagement and Retention: Drive employee engagement initiatives and foster a positive work culture.

HR Operations: Oversee daily HR operations (benefits administration, HRIS management, payroll reconciliation, Talent Acquisition, headcount planning / management, etc.). Ensure accurate and timely HR data management and reporting. Deploy continuous improvement initiatives that maximize HR programs, practices, and standard value. Leverage AI and Power BI where applicable to automate / reduce administrative tasks.

Other duties as assigned.

The Candidate\nDegree in Human Resources, Business Administration, or a related field. Master's degree preferred.

10+ years broad and progressive experience in human resources with 7+ years’ experience in management role.

Prior experience in site leadership position is required.

Proven experience as an HR leader in a manufacturing environment, ideally consumer health, food, medical devices, or pharmaceutical industry. CDMO experience highly preferred.

Solid knowledge of labor laws and regulations and excellent understanding of HR best practices, policies, and procedures.

Strong experience with change management efforts and employee engagement programs.

Ability to work effectively in a fast-paced, dynamic environment and ability to be on site 5 days a week.

Demonstratable leadership experience at Catalent (including but not limited to participation in Catalent-sponsored programs such as NGGL, GOLD, LEAD Now, GM Excellence, and GROW) may be considered in place of external experience

The anticipated salary range for this position in Maryland is $180,000 - 200,000 plus an annual bonus target. The final salary offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Catalent is a multi-state employer, and this salary range may not reflect positions that work in other states.\nWhy You Should Join Catalent\nDefined career path and annual performance review and feedback process

Diverse, inclusive culture

Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives

Dynamic, fast-paced work environment

Community engagement and green initiatives

Generous 401k match and paid time off accrual

Medical, dental, and vision benefits effective day one of employment

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.\nVisit Catalent Careers to explore career opportunities.\nCatalent is an Equal Opportunity Employer, including disability and veterans.\nIf you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations at catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.\nNotice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.\nImportant Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to spam at catalent.com for us to investigate with local authorities.\nCalifornia Job Seekers can find our California Job Applicant Notice HERE.

#J-18808-Ljbffr\n","Director, Human Resources

Position Summary\n100% onsite

Catalent is a leading global CDMO partnering with pharma and biotech innov...","Director, Human Resources",["B","2359323836"],"7 days ago","/jobs/2359323836-director-human-resources","/jobs?keyword=Director%2C+Human+Resources",{"_426":425,"_430":549,"_449":450,"_441":529,"_240":550,"_437":551,"_424":425,"_111":552,"_428":191,"_429":191,"_451":450,"_439":440,"_422":553,"_452":534,"_427":115,"_473":554,"_457":555,"_475":552,"_476":440,"_478":537,"_480":481,"_482":556},["D",1770386400000],"Position Summary

Shift: Monday – Friday 8am-5pm\n100% on-site\nCatalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life‑cycle supply. With time‑tested experience in development sciences, delivery technologies, and multi‑modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life‑enhancing and life‑saving treatments for patients annually.\nThe Human Resources Specialist supports day‑to‑day HR operations for a pharmaceutical manufacturing facility. Reporting directly to the Site’s Human Resources Director, this role provides hands‑on support in recruitment, onboarding, training coordination, employee relations, HR compliance, and HR administrative processes. The HR Specialist helps ensure the site maintains a strong, engaged workforce while meeting all regulatory, quality, and safety requirements.\nThe role

Support recruitment and workforce needs for hourly and salaried roles in partnership with the Talent Acquisition Center of Excellence and site HR leadership.\nLead and coordinate new‑hire onboarding, ensuring timely completion of GMP, safety, and HR documentation.\nServe as a first point of contact for employee questions regarding HR policies, benefits, and processes.\nMaintain accurate, compliant personnel files and HRIS data, including employee changes, attendance records, and reporting.\nAdminister site payroll accurately and support benefits and leave programs (FMLA, ADA, Leaves of Absence).\nAssist with employee relations matters, including investigations, documentation, and follow‑up actions as directed by site HR leadership.\nPartner with cross‑functional site teams and support continuous improvement initiatives and special HR projects.\nThe candidate

Bachelor's Degree in relevant discipline (e.g., Human Resources, Business Management or equivalent). Equivalent experience considered.\nMinimum 3+ years’ of human resources experience required.\nExposure to the pharmaceutical, healthcare, medical device, or related technical industries is highly preferred.\nStrong understanding of HR fundamentals, including recruitment, onboarding, payroll, and HR administration.\nExcellent communication, organizational, and time management skills.\nAdvanced PC skills, knowledge of company specific software packages, including HRIS.\nAbility to handle confidential information with professionalism and discretion.\nDemonstrated ability to read, write, and speak English.\nThe anticipated salary range for this position in Maryland is $77,000 - $92,000 plus an annual bonus target. The final salary offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Catalent is a multi‑state employer, and this salary range may not reflect positions that work in other states.\nWhy you should join Catalent

Competitive medical benefits and 401(k)\n152 hours PTO + 8 Paid Holidays\nDynamic, fast‑paced work environment\nOpportunity to work on Continuous Improvement Processes\nCatalent offers rewarding opportunities to further your career!

Join the global drug development and delivery leader and help us bring over 7,000 life‑saving and life‑enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.\nVisit Catalent Careers to explore career opportunities.\nCatalent is an Equal Opportunity Employer, including disability and veterans.

#J-18808-Ljbffr\n","Position Summary

Shift: Monday – Friday 8am-5pm\n100% on-site\nCatalent, Inc. is a leading global contract development and manufacturing org...","Human Resources Specialist",["B","2422955834"],"10 hours ago","/jobs/2422955834-human-resources-specialist","/jobs?keyword=Human+Resources+Specialist","actionData","errors"]