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$144.5K

How much do biopharma services jobs pay per year?

As of Aug 19, 2026, the average yearly pay for biopharma services in the United States is $68,281.00, according to ZipRecruiter salary data. Most workers in this role earn between $46,500.00 and $81,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in biopharma services, and why are they important?

To thrive in Biopharma Services, you need a solid background in life sciences, clinical research, and regulatory compliance, usually supported by a degree in biology, pharmacy, or a related field. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) certification, and laboratory data analysis tools is typically required. Strong attention to detail, effective communication, and project management skills help professionals excel in cross-functional teams and client interactions. These competencies ensure high-quality service delivery, regulatory adherence, and successful execution of complex biopharmaceutical projects.

What are some common challenges faced by professionals working in biopharma services, and how can they be addressed?

Professionals in biopharma services often encounter challenges such as adapting to rapidly changing regulatory requirements, managing complex projects with tight timelines, and ensuring clear communication among cross-functional teams. Staying updated with industry regulations, fostering strong project management skills, and actively collaborating with colleagues from diverse scientific and business backgrounds are key ways to address these challenges. Many organizations provide ongoing training and encourage teamwork, which helps professionals navigate these complexities and contribute effectively to drug development and clinical service projects.

What is the difference between Biopharma Services vs Biotech Research Associate?

AspectBiopharma ServicesBiotech Research Associate
Required CredentialsBachelor's degree in life sciences, relevant certificationsBachelor's or Master's in biology, biochemistry, or related fields
Work EnvironmentContract labs, CROs, pharmaceutical companiesResearch labs, biotech companies, academic institutions
Employer & Industry UsageUsed by contract research organizations and pharma firmsCommonly employed in biotech and research institutions
Search & Comparison IntentPeople comparing roles in biopharma industryIndividuals exploring research-focused biotech careers

Biopharma Services typically refers to roles within contract research organizations or pharmaceutical companies providing testing and development support. Biotech Research Associates focus on conducting experiments and research within biotech firms or academic labs. While both roles require a background in life sciences, Biopharma Services often involves client-facing or support functions, whereas Biotech Research Associates are more research-intensive.

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Biopharma Services jobs near you
Infographic showing various Biopharma Services job openings in the United States as of August 2026, with employment types broken down into 96% Full Time, and 4% Contract. Highlights an 87% In-person, 2% Hybrid, and 11% Remote job distribution, with an average salary of $68,281 per year, or $32.8 per hour.

Manufacturing Specialist - Filling, 3rd shift

INCOG BioPharma Services

Fishers, IN • On-site

Full-time

Re-posted 14 days ago

Job description

Description
The Manufacturing Specialist is a key technical role within INCOG BioPharma Operations. The ideal candidate must have experience in pharmaceuticals and/or biologics and GMP manufacturing.
The Manufacturing Specialist will be expected to work hands-on, be actively involved in continuous process improvements while taking ownership of the quality and quantity of product produced. The ideal candidate should possess a strong mechanical aptitude with strong trouble shooting skills on filling manufacturing equipment. They should demonstrate mentor and leadership skills to motivate manufacturing personnel, drive timely production activities and inspire problem solving & solution driven thinking.
This is a 3rd shift position with typical hours Sunday-Thursday from 11:00PM-7:30AM.
Essential Job Functions:
  • Follow production and manufacturing procedures.
  • Perform duties in Grade C, D, and controlled non-classified cleanrooms.
  • Perform aseptic manipulations within Grade A isolators.
  • Safely operate production equipment including setup and changeovers.
  • Lead batch start up activities and execution of production cycles
  • Accurately document data and complete batch records.
  • Execute validation/engineering protocols as needed.
  • Train others in various manufacturing tasks including, but not limited to: fill/finish, sanitization, component and equipment preparation.
  • Maintain production equipment and troubleshoot issues.
  • Support equipment optimization efforts and continuous improvement efforts.
  • Resolve issues that arise in day to day running of operation and providing timely responses and solutions.
  • SME for filling equipment and supporting systems.
  • Participate and/or support process FMEAs to understand process and product risks as a pre-requisite for process validation.
  • Provide technical support to manufacturing activities.
  • Apply Good Engineering Practices (GEP) to drive site engineering and operational excellence.
  • Work flexible hours to ensure production facility coverage.

Job Requirements:
  • High School diploma and 3 years of GMP pharmaceutical experience with the operation, cleaning, and maintenance of pharmaceutical GMP equipment.
  • Working knowledge of MS Office, MS Word, MS Excel, Windows or equivalent is required.
  • Must have previous experience with pharmaceutical aseptic processing (fill and finish) cGMP.

Additional Preferences:
  • BS in biological sciences/biotechnology and 1 year of GMP pharmaceutical experience with the installation, operation, cleaning, and maintenance of pharmaceutical GMP equipment.
  • Excellent communication skills.
  • Ability to apply concepts such as fractions, percentages, ratios and proportions to practical situations.
  • Ability to learn and operate a range of industry systems including and not limited to ERP and inventory management systems.

Additional info about INCOG BioPharma Services:
Additional info about INCOG BioPharma Services:
At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture and priorities are different by design: focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business.
If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus.
INCOG BioPharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at INCOG BioPharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics.
Qualified applicants must be authorized to work in the United States on a full-time basis. INCOG will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.
By submitting your resume and details, you are declaring that the information is correct and accurate.

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