Sr Associate I, Quality Control Microbiology

Posted 12 Days Ago
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Triangle Trailer Park, Township of Jacksonville, NC, USA
In-Office
81K-105K Annually
Senior level
Biotech
The Role
Lead and perform QC microbiology testing (bioburden, endotoxin, plate reading, microbial ID), environmental and utilities monitoring, review LIMS data, prepare EM/UM reports, troubleshoot assays, train staff, support method qualification, conduct investigations, and maintain lab readiness under GMP.
Summary Generated by Built In

Schedule: This onsite position operates on 10-hour shifts from Sunday through Wednesday during the first shift (8AM-6PM), with some occasional support required outside of those hours.

About This Role

We are seeking a highly motivated QC Microbiology Sr Associate I to support microbiological testing of in-process and raw materials, and environmental/utilities monitoring at RTP drug substance manufacturing facility. The Sr. Associate I is responsible for leading key operational aspects of the QC Microbiology laboratory. The Sr. Associate I performs and trains other team members on the microbial testing of all in-process drug substance, EM/UM, and raw materials samples. Additionally this role is responsible for method qualification and projects as assigned.

What You’ll Do

  • Review test data in LIMS

  • Prepare quarterly EM/UM reports

  • Supports testing for all qualification and study directed testing

  • Troubleshoot complex assays

  • Perform microbiology testing (e.g. Bioburden, Endotoxin, plate reading, and microbial identification) following standard procedures

  • Conduct routine Environmental Monitoring (viable and non-viable) in controlled manufacturing areas

  • Collect and process utility and compressed gas samples

  • Comply with SOPs and controlled documents under minimal supervision

  • Maintain laboratory cleanliness, equipment readiness, and inventory

  • Perform investigations (i.e. laboratory and deviations)

  • Follow site safety and contamination control policies

  • Work overtime as required by business needs

  • Perform other assigned duties

Who You Are

  • Someone who demonstrates strong attention to detail and analytical skills, along with a solid commitment to maintaining data integrity and quality

  • You possess a collaborative approach and work effectively across manufacturing and facilities teams

Required Skills

  • Bachelor’s in Microbiology, Biology, or related field

  • Minimum 4 years’ experience in pharmaceutical microbiology and GMP-regulated manufacturing

  • LIMS experience, including using electronic notebooks

  • Demonstrated knowledge of microbiological assays (bioburden, endotoxin, environmental monitoring), aseptic techniques, and general laboratory techniques

  • Experience with document control including reviewing and editing technical documents

  • Intermediate familiarity with fundamental statistical tools to analyze data in relation to trends results

  • Able to follow procedures and complete technical tasks

  • Can meet cleanroom and aseptic gowning requirements

  • Physically able to stand long periods, bend, move carts, and lift 25 lbs

  • Strong written and verbal communication skills, along with proficiency in Microsoft Word and Excel

  • Excellent organizational skills with the ability to prioritize, follow through on tasks, and meet deadlines

Preferred Skills

  • Advanced knowledge of Microbiology testing and Microbiology theory

  • Prior experience in utilities monitoring, including gas monitoring

  • Prior training experience, including classroom training

  • Proficient in using LIMS systems, Veeva, Kneat, and Microsoft software

  • Knowledgeable in GMP, GLP, and GDP requirements

  • Advanced knowledge of all compendial test methods (Bioburden, Endotoxin, Sterility testing)

  • LEAN lab and Six Sigma training and/or certification

  • Advanced experience with microbial ID systems, ability to troubleshoot complex equipment and instrumentation (MALDI, MicroSeq)

  • Experience performing EM/UM excursion investigations


 

Job Level: Professional


Additional Information

The base compensation range for this role is: $81,000.00-$105,000.00


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

Why Biogen?

We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.


At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our Biogen.


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.



Skills Required

  • Bachelor's in Microbiology, Biology, or related field
  • Minimum 4 years' experience in pharmaceutical microbiology and GMP-regulated manufacturing
  • LIMS experience, including using electronic notebooks
  • Demonstrated knowledge of microbiological assays (bioburden, endotoxin, environmental monitoring)
  • Aseptic techniques and general laboratory techniques
  • Experience with document control including reviewing and editing technical documents
  • Intermediate familiarity with fundamental statistical tools to analyze data and trends
  • Ability to follow procedures and complete technical tasks with minimal supervision
  • Can meet cleanroom and aseptic gowning requirements
  • Physically able to stand long periods, bend, move carts, and lift 25 lbs
  • Strong written and verbal communication skills
  • Proficiency in Microsoft Word and Excel
  • Excellent organizational skills with ability to prioritize and meet deadlines
  • Advanced knowledge of Microbiology testing and Microbiology theory
  • Prior experience in utilities monitoring, including gas monitoring
  • Prior training experience, including classroom training
  • Proficient in using LIMS systems, Veeva, Kneat, and Microsoft software
  • Knowledgeable in GMP, GLP, and GDP requirements
  • Advanced knowledge of compendial test methods (Bioburden, Endotoxin, Sterility testing)
  • LEAN lab and Six Sigma training and/or certification
  • Advanced experience with microbial ID systems and troubleshooting complex instrumentation (MALDI, MicroSeq)
  • Experience performing EM/UM excursion investigations

Biogen Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Biogen and has not been reviewed or approved by Biogen.

  • Fair & Transparent Compensation Pay is generally positioned as competitive and often perceived as fair across roles, with total compensation framed as strong when bonus and equity are included. Compensation sentiment is described as above-average overall, though it varies by function and business cycle.
  • Equity Value & Accessibility Equity programs are repeatedly highlighted as a meaningful part of the total package, including stock programs and an employee stock purchase plan. Equity and bonus elements are portrayed as important contributors to feeling well rewarded beyond base pay.
  • Leave & Time Off Breadth Time-off benefits are described as distinctive, including a year-end shutdown and a paid sabbatical after extended tenure. Vacation, holidays, sick time, and personal-significance days are also presented as supportive of work-life needs.

Biogen Insights

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The Company
HQ: Cambridge, MA
9,575 Employees
Year Founded: 1978

What We Do

Through cutting-edge science and medicine, Biogen discovers, develops and delivers innovative therapies worldwide for people living with serious neurological and neurodegenerative diseases. Founded in 1978, Biogen is a pioneer in biotechnology and today the Company has the leading portfolio of medicines to treat multiple sclerosis, has introduced the first and only approved treatment for spinal muscular atrophy, and is at the forefront of neurology research for conditions including Alzheimer’s disease, Parkinson’s disease and amyotrophic lateral sclerosis. Biogen also manufactures and commercializes biosimilars of advanced biologics. With approximately 7000 people worldwide, we are truly a global organization, headquartered in Cambridge, Massachusetts, which is also home to our research operations. Our international headquarters are based in Zug, Switzerland and we have world-class manufacturing facilities in North Carolina and Denmark. We offer therapies globally through direct affiliate presence in 30 countries and a network of distribution partners in over 50 additional countries. For more information, please visit www.biogen.com. Follow us on social media – Twitter, LinkedIn, Facebook, YouTube.

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