Manufacturing Specialist, Filling
Listed on 2026-07-21
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Manufacturing / Production
Pharmaceutical Manufacturing, Validation Engineer -
Pharmaceutical
Pharmaceutical Manufacturing, Validation Engineer
Manufacturing Specialist – Filling Summary
INCOG Bio Pharma is seeking a highly motivated individual with subject matter expert (SME) capabilities in sterile pharmaceutical manufacturing process controls and industrial automation. The Manufacturing Specialist is a key technical role within INCOG Bio Pharma Operations. The ideal candidate must have experience in pharmaceuticals and/or biologics, GMP manufacturing, or within highly regulated industries.
1st shift position with typical hours from Monday-Friday 7:00AM-3:30PMEssential Job Functions:
- Follow production and manufacturing procedures.
- Perform duties in Grade C, D, and controlled non-classified clean rooms.
- Perform aseptic manipulations within Grade A isolators.
- Perform cleaning and sanitization, equipment preparation, and aseptic filling duties as needed.
- Safely operate production equipment including setup and changeovers.
- 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.
- Collaborate and communicate with cross functional teams.
- Work flexible hours to ensure production facility coverage.
Job Requirements:
- 3 years of GMP pharmaceutical experience with the operation, cleaning, and maintenance of pharmaceutical filling equipment.
- Working knowledge of MS Office, MS Word, MS Excel, Windows or equivalent is required.
- BS in biological sciences/biotechnology and 1 year of GMP pharmaceutical experience with the installation, operation, cleaning, and maintenance of pharmaceutical GMP equipment.
- Demonstrated knowledge of pharmaceutical manufacturing of biotechnology products, aseptic processing (fill and finish) general Good Manufacturing Practices (cGMP).
- 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.
INCOG Bio Pharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at INCOG Bio Pharma 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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