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Process Science Associate Upstream Jobs (NOW HIRING)

BioTalent

Manufacturing Associate

Tustin, CA · On-site

... upstream processes such as cell culture, media/buffer preparation, bioreactors, seed train ... Additional Manufacturing Associate schedules may be available, so candidates with strong upstream ...

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How much do process science associate upstream jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for process science associate upstream in the United States is $29.18, according to ZipRecruiter salary data. Most workers in this role earn between $27.16 and $32.45 per hour, depending on experience, location, and employer.

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Infographic showing various Process Science Associate Upstream job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 15% Part Time, 3% Contract, and 1% Nights. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $60,696 per year, or $29.2 per hour.

Process Technician - Upstream operations

Exton, PA

LanceSoft Inc
Recruiting and Staffing Services • 1 - 5K employees
Learn more about LanceSoft Incexternal

Contractor

Re-posted 24 days ago

Key responsibilities

  • Execute routine operation, maintenance, and requalification of upstream production equipment in a cGMP biopharmaceutical pilot plant.

  • Participate in process performance sampling, in-process testing, and documentation to support manufacturing of biologics drug substances.

  • Assist in the validation, maintenance, re-qualification, and commissioning of upstream (cell culture and harvest) production equipment.

Job description

Company Description

LanceSoft - Pharmaceutical Client

Job Description

Under supervision and guidance, the Process Technician of Upstream Operations will be responsible for hand-on executing the routine operation, maintenance, and periodically requalification of cell culture based upstream production equipment and production suites in a cGMP biopharmaceutical pilot plant. In addition, the individual will execute and participate in the execution activities for scale-up and system operations supporting the manufacture of preclinical, clinical, and commercial biologics drug substances, including operation of cell culture bioreactors and harvest equipment, GMP documentation, and ensuring compliance to relevant regulations. 

Responsibilities Percent of Time 

Work in a hands-on capacity in the operation of upstream equipment for the manufacture of preclinical, clinical, and commercial biologics drug substances. 25
Ability to follow oral and written instructions, maintain neat, accurate, and current training and cGMP records.20
Performs all work duties via automated systems or manual operations in compliance with safe operating procedures, company and government regulations, and good manufacturing practices. 20
Perform process performance sampling/ in process testing supporting the manufacturing. 20
Maintains, inventories, and transports all required equipment, materials, supplies and products. Some heavy lifting is expected. 5
Participate and contribute in the validation maintenance, re-qualification of upstream (cell culture and harvest) production equipment. Assist and contribute in the commissioning of new equipment for upstream manufacturing. Participation in other areas within the facility may be added at the company's discretion. 5
Assist in equipment maintenance and calibration with appropriate internal departments. Provide cross-functional support for other departments within the pilot plant at the discretion of management. 5
The individual will play a hand-on execution role in the routine operation of the Biological pilot plant whose purpose is to produce material for preclinical, clinical, and commercial biologics drug substance to support Company's pipelines. Execution of manufacturing in the GMP production suites including documenting data compliantly.
Specifically, this person will participate and contribute to the success of the cell culture and harvest equipment operation and processes for the manufacture of materials for global clinical supplies. The individual will also participate in monitoring and maintaining the production area processes to remain compliant to regulations. The individual may also supporting a campaign and may provide cross-functional support for other departments within the pilot plant at the discretion of management.

Qualifications

Experience:
Minimum of 2-4 year (Associate degree) or 0-2 year (BS) practical scientific experience.
Ability to follow direction, work under supervision, and demonstrate capability in organizing complex activities in a cGMP production process.
Basic skills in executing routine production, maintenance, and operation of upstream cell culture and harvest equipment. Must have a Mechanical aptitude.
Good aseptic technique in maintaining process sterility.
Good written, communication, and interpersonal skills with the ability to work in a team environment required.
Capabilities in the operation of all area-specific production equipment such as large scale stir tank and/or single-use disposable bioreactors, centrifuge, micro-filtration, and CIP/SIP operations is a plus.
Previous exposures to cGMP, EMEA, and JP regulations as a plus.

Education: 

Two-year Associate degree or Four-year BS in Biotechnology or (Bio)Chemical Engineering or Engineering or Biological Sciences or equivalent job experience/degree is strongly preferred.

Additional Information

All your information will be kept confidential according to EEO guidelines.

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About LanceSoft

Sourced by ZipRecruiter

Established in 2000, LanceSoft is a Certified MBE and Woman-Owned organization. Lancesoft Inc. is one of the highest rated companies in the industry. We have been recognized as one of the Largest Staffing firms and ranked in the top 50 fastest Growing Healthcare Staffing firms in 2022. Lancesoft offers short- and long-term contracts, permanent placements, and travel opportunities to credentialed and experienced professionals throughout the United States. We pride ourselves on having industry leading benefits. We understand the importance of partnering with an expert who values your needs, which is why we're 100% committed to finding you an assignment that best matches your career and lifestyle goals. Our team of experienced career specialists takes the time to understand your needs and match you with the right job Lancesoft has been chosen by Staffing Industry Analysts as one of the Best Staffing Firms to Work for.LanceSoft specializes in providing Registered Nurses, Nurse Practitioners, LPNs/LVNs, Social Workers, Medical Assistants, and Certified Nursing Assistants to work in Acute Care Centers, Skilled Nursing Facilities, Long-Term Care centers, Rehab Facilities, Behavioral Health Centers, Drug & Alcohol Facilities, Home Health & Community Health, Urgent Care Clinics, and many other provider-based facilities.

Industry

Recruiting and staffing services

Company size

1,001 - 5,000 Employees

Headquarters location

Herndon, VA, US

Year founded

2000

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