Biopharmaceutical Manufacturing Associate II

Alphanumeric; King of Prussia (PA); Vor Ort; USD 28.000 - 40.000; Vollzeit

Zusammenfassung

Alphanumeric is hiring a Biopharmaceutical Manufacturing Associate II to support large‑scale biologics production in Upper Merion, PA. The role requires hands‑on cGMP manufacturing experience and involves operating manufacturing equipment while maintaining GMP documentation and safety standards.

You will work on 12‑hour shifts on a rotating schedule, onsite in King of Prussia with every other weekend, under a W2 contract.

Qualifikationen

• Bachelor's degree with cGMP manufacturing experience or related technical field.
• Associate's degree with cGMP manufacturing experience.
• High school diploma with at least 1 year of cGMP experience.

Aufgaben

• Perform daily cGMP manufacturing operations including fermentation, cell culture, chromatography and filtration.
• Operate and monitor automated equipment; maintain SOPs, batch records and GMP compliance.
• Document batch records accurately; identify deviations and escalate safety/quality concerns.
• Support equipment maintenance, autoclave ops, parts washing and clean‑up tasks.
• Collaborate with cross‑functional teams and support continuous improvement initiatives.

Ausbildung

BS/BA with cGMP manufacturing

AS in Biotechnology with cGMP

HS Diploma + 1 year cGMP

Tools

SAP

EBR (Electronic Batch Records)

Jobbeschreibung

Make Your Mark with a Job at Alphanumeric

Job Details

Biopharmaceutical Manufacturing Associate II
King of Prussia, PA
Posted: 11/11/2026
Job Description
Job ID#: 8439
Positions Available: 10

Biopharmaceutical Manufacturing Associate II - GMP Manufacturing

Location: Upper Merion / King of Prussia, PA
Pay Rate: $24.50/hour (Fixed)
Schedule: 12-hour shifts | 5:00 AM-5:00 PM or 5:00 PM-5:00 AM
Work Arrangement: Onsite | Rotating 3-4 shifts per week, including every other weekend
Employment Type: W2 Contract

Position Overview

Alphanumeric is hiring a Biopharmaceutical Manufacturing Associate II to support pharmaceutical manufacturing operations at a leading global biopharmaceutical organization in Upper Merion, PA. This is an excellent opportunity for candidates with hands‑on cGMP manufacturing experience who want to expand their technical skills in biologics production while contributing to the manufacture of life‑changing medicines. In this role, you will support large‑scale biopharmaceutical production activities, operate and monitor manufacturing equipment, maintain accurate GMP documentation, and collaborate with cross‑functional teams to ensure safe, compliant, and efficient manufacturing operations.

Responsibilities

• Perform daily cGMP manufacturing operations, including fermentation, cell culture, solution preparation, chromatography, filtration, and concentration processes.
• Support autoclave operations, parts washing, equipment preparation, and production area cleaning.
• Operate and monitor automated manufacturing equipment, ensuring critical process parameters remain within established specifications.
• Execute manufacturing activities in accordance with Standard Operating Procedures (SOPs), batch records, and GMP requirements.
• Complete accurate and timely manufacturing documentation, including electronic batch records, logbooks, and production data.
• Identify and elevate equipment abnormalities, process deviations, and potential safety or quality concerns.
• Participate in troubleshooting, investigations, and continuous improvement initiatives.
• Support engineering, validation, and technology transfer activities as needed.
• Coordinate with production teams to ensure equipment, materials, and supplies are available to meet manufacturing schedules.
• Develop proficiency across multiple manufacturing operations through training and collaboration with senior team members.
• Maintain compliance with safety, quality, and data integrity standards.

Required Qualifications

• Candidates must meet one of the following education and experience combinations:
• Bachelor's degree (BS/BA) with cGMP manufacturing experience; OR
• Associate's degree in Biotechnology or a related technical field from Montgomery County Community College, with cGMP manufacturing experience; OR
• High school diploma or equivalent with at least1 year of cGMP manufacturing experience.

Preferred Qualifications

• Previous experience in pharmaceutical, biotechnology, or biologics manufacturing.
• Familiarity with upstream or downstream bioprocessing operations, including cell culture, fermentation, chromatography, or filtration.
• Experience working with automated manufacturing equipment.
• Knowledge of GMP documentation, batch records, and data integrity requirements.
• Familiarity with SAP, Electronic Batch Records (EBR), or other digital manufacturing systems.
• Strong attention to detail and ability to follow complex manufacturing instructions.
• Effective written and verbal communication skills.
• Ability to work collaboratively in a team-oriented production environment.
• Demonstrated commitment to safety, quality, accountability, and continuous improvement.

Work Schedule and Requirements

• 12-hour shifts: 5:00 AM-5:00 PM or 5:00 PM-5:00 AM.
• Rotating schedule averaging 3-4 shifts per week.
• Must be available to work every other weekend.
• Position requires working onsite in Upper Merion, PA.
• Candidates must be comfortable working in a regulated pharmaceutical manufacturing environment.
• Fixed pay rate: $24.50/hour.

Why Join Alphanumeric?

At Alphanumeric, we connect talented professionals with meaningful opportunities at leading organizations in the pharmaceutical and biotechnology industries. Established in 1979, Alphanumeric supports life sciences and healthcare organizations around the world. We are committed to creating meaningful connections, supporting professional growth, and helping our employees make a difference. Join a team dedicated to manufacturing excellence and helping bring life‑changing medicines to patients.

Equal Employment Opportunity

Alphanumeric is an equal opportunity employer and considers all qualified applicants without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information, or any other characteristic protected by applicable law. If you require a reasonable accommodation during the application or interview process, please contact our recruiting team at [e-mail]. Please Note: We are unable to accept applications from third‑party agencies for this position. Candidates must be eligible to work directly on Alphanumeric's W2 without requiring employment sponsorship now or in the future.