Our client, a well-established, pharmaceutical organization is hiring an Associate Director of Manufacturing (Quality Assurance) with the opportunity to grow in a specialized manufacturing facility. The ideal candidate has:

Pharmaceutical Manufacturing Experience (in oral solid dosages)
Supporting manufacturing from the quality perspective
An understanding of quality on the floor or experience working on the floor

This role will be a leader in an organization that continues to grow and establish themselves as a global leader. Responsibilities include, but are not limited to:

Support the continuous improvement of manufacturing quality systems and processes.
Provide QA oversight for all manufacturing operations
Review and approve manufacturing batch records, line clearance documentation, and associated QA forms.
Train and mentor QA personnel and manufacturing operators on quality-related topics.
Oversee and (commonly) author investigation of manufacturing deviations, non-conformances, and out-of-specification (OOS) results.

The ideal candidate would have 8–10 years of progressive experience in pharmaceutical manufacturing quality assurance or quality systems.

This role does require relocation to the facility located in the Midwest.

","

Our client, a well-established, pharmaceutical organization is hiring an Associate Director of Manufacturing (Quality Assurance) with the opport...","Senior Production Manager",[89],["B","3522683763"],"Work at Germer International - Pharmaceutical Recruiting","3 days ago","/jobs/3522683763-senior-production-manager","Omaha, NE, United States","/jobs?keyword=Germer+International+-+Pharmaceutical+Recruiting","/jobs?location=Omaha%2C+NE%2C+United+States","/jobs?keyword=Senior+Production+Manager",{"_65":66,"_67":90,"_69":91,"_71":92,"_73":93},"Omaha","Omaha, NE, United States, 68197","NE","68197",["D",1777377600000],"Irrespub","Overview

The Formulation Sciences Program and laboratory of Dr. Brooke Bernhardt at St. Jude Children's Research Hospital is recruiting a motivated postdoctoral researcher. The post‑doc will be part of a new program in Formulation Sciences which aims to develop and translate pediatric‑suitable dosage forms for clinical care and research. We are a translational research program that aims to have direct impact on patient care and clinical trials. Our program leverages 3D printing (primarily semi‑solid extrusion) as the mechanism for reformulating existing pharmaceuticals – both active pharmaceutical ingredients and finished dosage forms – into novel dosage forms.
Responsibilities

Develop and translate pediatric‑suitable dosage forms using 3D printing and formulation development.
Reformulate existing pharmaceuticals – both active pharmaceutical ingredients and finished dosage forms – into novel dosage forms.
Conduct in‑process and post‑production testing of finished dosage forms according to United States Pharmacopoeia guidance.
Qualifications

Earned or expected to earn a PhD in a relevant field (e.g., Pharmaceutical Sciences, Textile Engineering, Chemical Engineering).
Strong skills in formulation sciences/clinical pharmaceutics.
Project management and scientific writing experience.
Excellent communication skills and a collaborative attitude.
Experience with 3D printing and clinical pharmaceutics/formulation development.
EEO Statement

St. Jude is an Equal Opportunity Employer.

#J-18808-Ljbffr
","Overview

The Formulation Sciences Program and laboratory of Dr. Brooke Bernhardt at St. Jude Children's Research Hospital is recruiting a ...","Postdoctoral Research Associate",[108],["B","3522909568"],"Work at Irrespub","19 hours ago","/jobs/3522909568-postdoctoral-research-associate","Memphis, TN, United States","/jobs?keyword=Irrespub","/jobs?location=Memphis%2C+TN%2C+United+States","/jobs?keyword=Postdoctoral+Research+Associate",{"_65":66,"_67":109,"_69":110,"_71":111,"_73":112},"Memphis","Memphis, TN, United States, 37544","TN","37544",["D",1777262400000],"Allergan","Purpose
Serves as a process engineering subject matter expert responsible for the development, optimization, and technology transfer of oral solid dosage form (OSD) drug products within a pharmaceutical manufacturing environment. This position independently investigates and resolves complex manufacturing process challenges, drives continuous improvement of OSD unit operations, and supports the seamless transfer of new and existing products from R&D to global manufacturing sites and third-party manufacturers (TPMs). The role applies deep technical knowledge of OSD processing—including granulation, blending, compression, coating, and encapsulation—to ensure robust, scalable, and compliant manufacturing processes across the product lifecycle.

Responsibilities

Lead process engineering activities for OSD drug products, including development, scale-up, validation, and technology transfer to internal and external (TPM) manufacturing sites.

Design, execute, and interpret process development and optimization experiments for OSD unit operations such as wet/dry granulation, high-shear mixing, fluid bed processing, roller compaction, tablet compression, film coating, and capsule filling.

Apply first-principles engineering and Quality by Design (QbD) methodologies to establish process understanding, define critical process parameters (CPPs), and link them to critical quality attributes (CQAs) for OSD products.

Author and review technical documents including process descriptions, batch records, validation protocols and reports, tech transfer packages, and regulatory submissions (e.g., CMC sections of INDs/NDAs/ANDAs).

Troubleshoot and resolve manufacturing deviations, process failures, and equipment-related issues at commercial OSD manufacturing facilities through root cause analysis and implementation of corrective actions.

Collaborate cross-functionally with R&D, Analytical Sciences, Quality, Regulatory Affairs, and Supply Chain to ensure successful product lifecycle management from development through commercialization.

Evaluate and implement new OSD processing technologies and equipment to improve process efficiency, product quality, and manufacturing robustness.

Develop and maintain productive working relationships with global manufacturing partners, engineering teams, and external contract organizations to support OSD product transfers and launches.

Set and manage project timelines for process engineering deliverables; provide technical leadership and mentorship to junior scientists and engineers on OSD process-related topics.

Routinely review and apply relevant scientific and engineering literature to advance OSD process development capabilities and identify innovative solutions to technical challenges.

Qualifications

BS or equivalent education with typically 7 or more years of experience or MS or equivalent education with typically 5 or more years of experience.

Demonstrated ability to independently design, execute and interpret critical experiments to answer scientific questions.

Demonstrated ability to learn, understand and master new experimental techniques.

Ability to multitask and work within timelines.

Demonstrated scientific writing skills and strong verbal communication skills.

Additional Information

The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.

We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.

This job is eligible to participate in our short-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company’s sole and absolute discretion until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html

#J-18808-Ljbffr
","Purpose
Serves as a process engineering subject matter expert responsible for the development, optimization, and technology transfer of oral so...","Scientist, Engineering II, Oral Solid Dosage",[127],["B","3523581355"],"Work at Allergan","2 days ago","/jobs/3523581355-scientist-engineering-ii-oral-solid-dosage","North Chicago, IL, United States","/jobs?keyword=Allergan","/jobs?location=North+Chicago%2C+IL%2C+United+States","/jobs?keyword=Scientist%2C+Engineering+II%2C+Oral+Solid+Dosage",{"_65":66,"_67":128,"_69":129,"_71":130,"_73":131},"North Chicago","North Chicago, IL, United States, 60086","IL","60086",["D",1777345200000],"Thermo Fisher Scientific","This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.
Work Schedule
Standard (Mon-Fri)

Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description
Quality Project Lead

Division / Site Specific Information

With the support of over 800 talented employees, Thermo Fisher Scientific’s

Oral Solid Dose (OSD) site in Cincinnati, Ohio

provides comprehensive drug development and commercial manufacturing services. The site specializes in advanced dosage forms including controlled and sustained release products, osmotic release dosage forms (laser drilling), liquid-filled hard capsules, controlled substances, and abuse-deterrent technologies.
Discover Impactful Work

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. In this role, you will help ensure the highest quality standards across our operations, supporting our Mission to enable our customers to make the world healthier, cleaner, and safer. As a

Quality Specialist III , you will collaborate cross-functionally to strengthen quality systems, drive continuous improvement, and ensure regulatory compliance in a highly regulated pharmaceutical manufacturing environment.
A Day in the Life

Maintain quality systems in compliance with cGMPs, GxP regulations, ISO standards, global regulatory requirements, and company policies

Lead and support investigations related to deviations, nonconformances, and quality events using sound root cause analysis techniques

Manage and support CAPA, change control, and risk assessment activities

Author, review, and approve SOPs, investigation reports, and quality documentation

Conduct and host internal audits, external audits, and regulatory inspections

Analyze quality data, perform trending, and report quality metrics to support continuous improvement

Collaborate with cross-functional teams to implement corrective and preventive actions

Foster a culture of quality excellence and continuous improvement across the organization

Keys to Success

Education
Advanced Degree with a minimum of 3 years of experience

OR

Bachelor’s Degree with a minimum of 5 years of experience

Preferred fields of study: Life Sciences, Engineering, Chemistry, Biology, or related technical discipline

Experience
Experience in quality assurance or quality control within regulated industries (pharmaceutical, biotech, or medical device preferred)

Proven experience with CAPA, deviation management, change control, and quality management systems

Experience conducting and hosting internal and external audits and regulatory inspections

Project management experience preferred

Knowledge, Skills, and Abilities
Knowledge
Strong knowledge of GMP/GxP regulations and ISO standards (9001/13485)

Understanding of risk assessment methodologies and continuous improvement tools

Skills
Proficiency with quality systems software (e.g., TrackWise, document control systems)

Strong technical writing skills for SOPs, investigations, and quality reports

Proficiency in statistical analysis, data trending, and quality metrics reporting

Strong verbal and written communication skills

Abilities
Advanced problem-solving and root cause analysis capabilities

Ability to work independently and guide cross-functional teams

Strong interpersonal skills with the ability to collaborate across functions and levels

High attention to detail and commitment to quality excellence

Physical Requirements / Work Environment

Ability to work in a pharmaceutical manufacturing environment

Ability to wear appropriate personal protective equipment (PPE) as required

Benefits

Thermo Fisher Scientific offers competitive remuneration, an annual incentive plan, and comprehensive benefits starting Day 1, including:
Medical, Dental, and Vision Insurance

Paid Time Off and Designated Paid Holidays

Retirement Savings Plan

Tuition Reimbursement

Relocation assistance is not provided
Must be legally authorized to work in the United States without sponsorship
Must be able to pass a comprehensive background check, including a drug screening
Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization and outstanding career and development opportunities. Our culture is built on integrity, intensity, involvement, and innovation.
","This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business comm...","Quality Project Lead",[146],["B","3523122878"],"Work at Thermo Fisher Scientific","1 days ago","/jobs/3523122878-quality-project-lead","Cincinnati, OH, United States","/jobs?keyword=Thermo+Fisher+Scientific","/jobs?location=Cincinnati%2C+OH%2C+United+States","/jobs?keyword=Quality+Project+Lead",{"_65":66,"_67":147,"_69":148,"_71":72,"_73":149},"Cincinnati","Cincinnati, OH, United States, 45208","45208",1072,"name","Hearst Television","agency","logo","slug","hearst-television","

Every career with Hearst Television is like a story. How it develops, where it takes you, the milestones you reach along the way – you’ve got a lot to look forward to as your unique career story unfolds. Hearst Television, a subsidiary of Hearst, owns and operates local television and radio stations serving nearly three dozen U.S. cities, reaching 24 million U.S. television households. Through its partnership with nearly all major networks, Hearst Television distributes national content across more than 120 video channels, including programming from ABC, NBC, CBS, CW, MY Net, MeTV, This TV, Estrella, and more. Hearst Television is recognized as one of the industry's premier companies. It has been honored with numerous awards for distinguished journalism and industry innovation, including the Walter Cronkite Award for political journalism, the national Edward R. Murrow Award, the DuPont-Columbia Award, and the George Foster Peabody Award.

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Job Description: Responsibilities: Follow Master Batch Records for the manufacturing of controlled, oral solid dose (OSD) and other dosage forms when required.

","descriptionText","Manufacturing Pharmaceutical Technician Cynet Systems Job Title Job Description: Responsibilities: Follow Master Batch Records for the manufacturing of controlled, oral solid dose (OSD) and other dosage forms when required.","Job Title

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Join the leading career community for creative, marketing, and media professionals.","Sign Up | Creative, Marketing & Media Job Search",{"_36":297},{"_151":31,"_284":296},{"_290":291,"_292":293,"_294":295},"href","https://www.mediabistro.com/create-alert","rel","canonical","tagName","link","Never miss an opportunity. Sign up for free email alerts and get the latest jobs in social media, graphic design, writing, and marketing delivered to your inbox.","Create Job Alerts | Media, Marketing & Creative Job Alerts",[395,396],{"_36":393,"_354":394,"_31":39},"unlimitedJobsEmail","clients@mediabistro.com","enterpriseCta",{"_389":390,"_391":392},{"_385":386,"_387":386,"_388":386},"mediaBoardSection",{"_36":375,"_354":376,"_31":377,"_378":379,"_373":380},"rolesSection",{"_36":370,"_354":371,"_31":372,"_373":374},"testimonialsSection",{"_36":367,"_354":368,"_31":369},"testimonials",[355,356,357],"employersSection",{"_36":353,"_354":243},"employerLogos",[317,318,319,320,321,322,323,324,325,326,327,328],{"_151":351,"_330":352},{"_151":349,"_330":350},{"_151":347,"_330":348},{"_151":345,"_330":346},{"_151":343,"_330":344},{"_151":341,"_330":342},{"_151":339,"_330":340},{"_151":337,"_330":338},{"_151":335,"_330":336},{"_151":152,"_330":334},{"_151":332,"_330":333},{"_151":329,"_330":331},"Leaf Group","image","https://production-rails-default.s3.us-east-2.amazonaws.com/public/post-jobs-logos/leaf-group-400x200.png","Cox Enterprises","https://production-rails-default.s3.us-east-2.amazonaws.com/public/post-jobs-logos/cox-enterprises-400x200.png","https://production-rails-default.s3.us-east-2.amazonaws.com/public/post-jobs-logos/hearst-television-400x200.png","Future","https://production-rails-default.s3.us-east-2.amazonaws.com/public/post-jobs-logos/future-400x200.png","Fox Corporation","https://production-rails-default.s3.us-east-2.amazonaws.com/public/post-jobs-logos/fox-corporation-400x200.png","Penguin Random House","https://production-rails-default.s3.us-east-2.amazonaws.com/public/post-jobs-logos/penguin-random-house-400x200.png","Springer Nature","https://production-rails-default.s3.us-east-2.amazonaws.com/public/post-jobs-logos/springer-nature-400x200.png","Penske Media Corporation","https://production-rails-default.s3.us-east-2.amazonaws.com/public/post-jobs-logos/penske-media-corporation-400x200.png","Dotdash","https://production-rails-default.s3.us-east-2.amazonaws.com/public/post-jobs-logos/dotdash-400x200.png","Meredith","https://production-rails-default.s3.us-east-2.amazonaws.com/public/post-jobs-logos/meredith-400x200.png","Bloomberg","https://production-rails-default.s3.us-east-2.amazonaws.com/public/post-jobs-logos/bloomberg-400x200.png","NBCUniversal","https://production-rails-default.s3.us-east-2.amazonaws.com/public/post-jobs-logos/nbc-universal-400x200.png","Media and Creative Employers on","subtitle",{"_358":364,"_360":365,"_154":366},{"_358":351,"_360":363,"_154":352},{"_358":359,"_360":361,"_154":362},"company","The Taunton Press","quote","What we like best about Mediabistro is the quality of targeted talent they deliver through their job board portal. We know we'll find the right type of talent for specialized positions that may be more challenging to fill. For almost fifteen years, Mediabistro has been our go-to resource for talent in the media/publishing space.","https://production-rails-default.s3.us-east-2.amazonaws.com/public/post-jobs-logos/taunton-press-400x200.png","Mediabistro is valuable partner when it comes to finding top candidates in the media industry. Their team is extremely responsive, which makes the posting process quick and easy. They also offer great insight into branding company pages.","Huffpost","I love using Mediabistro for my harder to fill creative roles. Multimedia positions like photo editors, video producers, or even niche journalists yield great results. Other job boards don't always produce the specialized talent my hiring teams are looking for, and I feel like I can find that talent through Mediabistro.","https://production-rails-default.s3.us-east-2.amazonaws.com/public/post-jobs-logos/huff-post-400x200.png","Trusted by Leading Media","and Creative Employers","See why top publishers, agencies, and brands rely on us to find exceptional talent.","Hire Remote and Local Talent","Across Every Media Vertical","Whether you are building an in-office team or seeking remote talent, access a specialized network of professionals in editorial, publishing, influencer marketing, and AI content strategy. Find candidates—from prompt engineers to production leads—who are ready to contribute from anywhere.","imageAlt","Media roles infographic","The #1 Destination for Media","and Creative Talent","Connect with top-tier full-time and freelance media professionals. Whether you are a leading publisher, a streaming service, or a growing brand, we deliver specialized talent you won't find on generalist job boards. Find your perfect match for:","bullets",[381,382,383,384],"Job seekers and featured job cards collage","News, Journalism & Book Publishing","Content Marketing, AI Prompt Engineering & Copywriting","Influencer Management, TV & Video Production","PR, Non-Profits & Education","showMediaBoardSection",true,"showRolesSection","showPlanIcon","text","*Unlimited plan is for direct employers only. Hiring at scale, posting on behalf of clients, or distributing across job boards?","linkText","Contact us for custom volume pricing, multi-brand support, and programmatic distribution.","The #1 Job Board for Media, Marketing & Creative Talent","Skip the unqualified resumes. 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