Manufacturing Associate II
NCBiotech, Durham, NC, United States
About This Role
Our factories run a basic 4‑10 Mon – Thurs model with the necessity to be flexible. Our manufacturing teams work 6am – 4pm with daily flexibility needed as well.
Shift Details
This role has our manufacturing teams work 6am – 4pm with daily flexibility needed as well.
Roles
Our Manufacturing Associates perform processing steps and manufacturing support activities in our Drug Substance facility in Research Triangle Park (RTP). These teams are the backbone of our operations – each playing a critical role in delivering our therapies to the patients who need them.
Our teams are organized by the steps in the biomanufacturing process that they operate in; including – Upstream (Synthesis), Downstream (Purification), and Solution Preparation. Manufacturing Associates perform these critical steps in a clean environment governed by Current Good Manufacturing Practices (cGMP).
Upstream / Synthesis
Buffer weigh outs
Amedite preparation
Synthesis operation using Unicorn operating system
Downstream / Purification
Column Chromatography
Detritalization
Ultra-Filtration
Bulk Dispensing of the drug substance
What You’ll Do
Execute daily manufacturing activities by operating production equipment, performing process steps, and completing validation or qualification protocols in accordance with cGMP and Standard Operating Procedures (SOPs)
Document all manufacturing work accurately, including cGMP data, deviations, equipment usage, and processing details. Create, revise, and maintain batch records, SLRs, equipment logbooks, and other key documentation
Support in‑process sampling and analysis, including routine measurements such as pH, conductivity, protein concentration, osmolality, and cell counts
Maintain a clean, safe, and audit‑ready workspace by following safety guidelines, good housekeeping practices, and compliance expectations
Collaborate as a reliable team member, showing up with focus, accountability, and a willingness to support teammates and shared goals
Participate in training and development, building your own capabilities while helping strengthen the skills and readiness of the team
Who You Are
You’re driven by a mission to save lives and bring a deep sense of purpose to the work you do. Biomanufacturing is complex, and you thrive in fast‑paced environments where learning agility, problem‑solving, and adaptability are essential.
Required Skills
The following combination of academic and/or relevant experience may be considered:
Bachelor’s degree, BioWorks Certificate, or associate’s degree from an accredited college, university, or program
High School Diploma (or equivalent) and at minimum of 6 months of direct experience
Experience in cGMP manufacturing, biotech, or pharmaceutical operations
Ability to follow detailed procedures and uphold safety and compliance standards
Familiarity with operating production equipment and maintaining manufacturing documentation
Preferred Skills
Bachelor’s degree in Science, Technology, Engineering and Mathematics (STEM) from an accredited college or university
Strong communication skills and a team‑oriented mindset
Job Level
Entry Level
Additional Information
The base compensation range for this role is: $23.56–$30.77.
Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.
Regular employees are eligible to receive both short term and long term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.
In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees’ and their families physical, financial, emotional, and social well‑being; including, but not limited to:
Medical, Dental, Vision, & Life insurances
Fitness & Wellness programs including a fitness reimbursement
Short- and Long-Term Disability insurance
A minimum of 15 days of paid vacation and an additional end‑of‑year shutdown time off (Dec 26-Dec 31)
Up to 12 company paid holidays + 3 paid days off for Personal Significance
80 hours of sick time per calendar year
Paid Maternity and Parental Leave benefit
401(k) program participation with company matched contributions
Employee stock purchase plan
Tuition reimbursement of up to $10,000 per calendar year
Employee Resource Groups participation
EEO Statement
All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.
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Our factories run a basic 4‑10 Mon – Thurs model with the necessity to be flexible. Our manufacturing teams work 6am – 4pm with daily flexibility needed as well.
Shift Details
This role has our manufacturing teams work 6am – 4pm with daily flexibility needed as well.
Roles
Our Manufacturing Associates perform processing steps and manufacturing support activities in our Drug Substance facility in Research Triangle Park (RTP). These teams are the backbone of our operations – each playing a critical role in delivering our therapies to the patients who need them.
Our teams are organized by the steps in the biomanufacturing process that they operate in; including – Upstream (Synthesis), Downstream (Purification), and Solution Preparation. Manufacturing Associates perform these critical steps in a clean environment governed by Current Good Manufacturing Practices (cGMP).
Upstream / Synthesis
Buffer weigh outs
Amedite preparation
Synthesis operation using Unicorn operating system
Downstream / Purification
Column Chromatography
Detritalization
Ultra-Filtration
Bulk Dispensing of the drug substance
What You’ll Do
Execute daily manufacturing activities by operating production equipment, performing process steps, and completing validation or qualification protocols in accordance with cGMP and Standard Operating Procedures (SOPs)
Document all manufacturing work accurately, including cGMP data, deviations, equipment usage, and processing details. Create, revise, and maintain batch records, SLRs, equipment logbooks, and other key documentation
Support in‑process sampling and analysis, including routine measurements such as pH, conductivity, protein concentration, osmolality, and cell counts
Maintain a clean, safe, and audit‑ready workspace by following safety guidelines, good housekeeping practices, and compliance expectations
Collaborate as a reliable team member, showing up with focus, accountability, and a willingness to support teammates and shared goals
Participate in training and development, building your own capabilities while helping strengthen the skills and readiness of the team
Who You Are
You’re driven by a mission to save lives and bring a deep sense of purpose to the work you do. Biomanufacturing is complex, and you thrive in fast‑paced environments where learning agility, problem‑solving, and adaptability are essential.
Required Skills
The following combination of academic and/or relevant experience may be considered:
Bachelor’s degree, BioWorks Certificate, or associate’s degree from an accredited college, university, or program
High School Diploma (or equivalent) and at minimum of 6 months of direct experience
Experience in cGMP manufacturing, biotech, or pharmaceutical operations
Ability to follow detailed procedures and uphold safety and compliance standards
Familiarity with operating production equipment and maintaining manufacturing documentation
Preferred Skills
Bachelor’s degree in Science, Technology, Engineering and Mathematics (STEM) from an accredited college or university
Strong communication skills and a team‑oriented mindset
Job Level
Entry Level
Additional Information
The base compensation range for this role is: $23.56–$30.77.
Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.
Regular employees are eligible to receive both short term and long term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.
In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees’ and their families physical, financial, emotional, and social well‑being; including, but not limited to:
Medical, Dental, Vision, & Life insurances
Fitness & Wellness programs including a fitness reimbursement
Short- and Long-Term Disability insurance
A minimum of 15 days of paid vacation and an additional end‑of‑year shutdown time off (Dec 26-Dec 31)
Up to 12 company paid holidays + 3 paid days off for Personal Significance
80 hours of sick time per calendar year
Paid Maternity and Parental Leave benefit
401(k) program participation with company matched contributions
Employee stock purchase plan
Tuition reimbursement of up to $10,000 per calendar year
Employee Resource Groups participation
EEO Statement
All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.
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