Manufacturing Specialist- Filling, 2nd shift

incog; Fishers (IN); On-site; USD 52,000 - 78,000; Full time

Job summary

INCOG BioPharma, based in Fishers, IN, seeks a Manufacturing Specialist – Filling (2nd shift) to set up and operate sterile filling equipment. You will document batch records, perform aseptic manipulations, and drive continuous improvements in a highly regulated environment.

The role requires GMP pharmaceutical experience, strong mechanical aptitude, and leadership to mentor manufacturing staff. You will collaborate with cross-functional teams and support production coverage on the 2nd shift at

Qualifications

• Minimum 3 years GMP pharma experience with filling equipment.
• Proficient in MS Office (Word, Excel) and Windows.

Responsibilities

• Follow production and manufacturing procedures.
• Operate production equipment; setup and changeovers.
• Document data and batch records.
• Train others in filling, sanitization, and equipment prep.
• Support continuous improvement and issue troubleshooting.
• Collaborate with cross-functional teams and cover shifts.

Skills

GMP experience

Troubleshooting

Leadership

Aseptic filling

Education

High School diploma

BS in Biotechnology

Tools

ERP systems

Inventory systems

MS Office

Job description

Manufacturing Specialist – Filling (2nd shift) Summary

INCOG BioPharma 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 BioPharma Operations. The ideal candidate must have experience in pharmaceuticals and/or biologics, GMP manufacturing, or within highly regulated industries.

The Manufacturing Specialist’s primary responsibility is to efficiently and safely set up and operate various pieces of production equipment within the facility. They 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 manufacturing equipment. They should demonstrate mentor and leadership skills to motivate manufacturing personnel, drive timely production activities and inspire problem solving & solution driven thinking.

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.
• 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:

• High School diploma and 3 years of GMP pharmaceutical experience with the installation, operation, cleaning, and maintenance of pharmaceutical filling equipment.
• Working knowledge of MS Office, MS Word, MS Excel, Windows or equivalent is required.

Job Preferences:

• 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.

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.