Manufacturing Associate I

PSC Biotech® Corporation; York (York County); On-site; USD 42,000 - 63,000; Full time

Benefits offered by this job

Overtime eligible

Medical and Sick Time benefits

Job summary

BioTechnique is seeking a role in sterile injectable manufacturing to perform complex tasks under GMP/ISO guidelines. The position involves aseptic and non-aseptic filling, equipment prep, and formulation activities with potential cross-departmental support.

The candidate should have a High School Diploma with 1–2 years of related manufacturing experience in an FDA-regulated facility, and be comfortable with variable shifts and documentation practices.

Qualifications

• High School Diploma with 1-2 years of work experience in a mechanically based or similar role.
• 1-2 years of professional manufacturing experience in an FDA Regulated Pharmaceutical facility preferred.
• Experience reviewing and creating controlled documents preferred.
• Experience with sterile injectable drugs preferred.

Responsibilities

• Perform aseptic and non-aseptic filling and equipment prep under GMP/ISO standards.
• Assist in formulation, fill activities, and cleaning/in-place operations.
• Maintain proper documentation including batch records and GDP adherence.
• Support engineering, warehouse and facilities as needed and work with cross-functional teams.

Skills

Strong communication skills

Attention to detail

Organizational skills

Analytical skills

Education

High School Diploma

Tools

MS Office/Excel

Job description

BioTechnique is a sterile injectable full service CDMO providing cytotoxic and therapeutic sterile injectable fill-finish services. From IND applications through commercial scale production, we provide formulation and compounding, fill-finish, and lyophilization services for a wide variety of liquid injectables. BioTechnique utilizes our team’s expertise to create a process design for our clients’ products that best suits their needs.

The Experience

With operations spanning the globe and featuring a multi-cultural team, BioTechnique is passionate about bringing the best and brightest together in an effort to form something truly special. When you make the decision to join our team, you will be offered the ability to feel inspired in your career, explore your professional passions, and work alongside a group of people who will value and nurture your talents. We are firm believers in coaching and developing the next generation of industry leaders and influencers. As such, you will not only be offered a compensation and benefits structure that rewards you but also be provided with the tools that will help you grow and learn. At BioTechnique, it’s about more than just a job—it’s about your career and your future.

Your Role

This position is responsible for performing a variety of complex tasks under general guidance and in accordance with the manufacturing instruction set and current GMP/ISO requirement and standards as defined in FDA and EU applicable Regulations. With general supervision the individual will perform routine and critical manufacturing operations, including but not limited to work functions in aseptic and non-aseptic filling, equipment prep, cleaning dissolution and formulation activities. The individual may provide support in other departments within the company, including but not limited to, engineering, warehouse and facilities. This is a W2 temporary position through January 29, 2027 with potential FTE extension. Shifts are expected to begin as Friday–Sunday, however, candidates must be able to commit to variable shifts including weekdays, evenings, weekend-focused schedules, or 7-day rotating schedule for the duration of the position.

• Maintain certification for aseptic gowning and demonstrate the ability to perform all duties using proper aseptic technique.
• Perform equipment preparation, including CIP (Clean-in-Place) and SIP (Steam-in-Place) operations, to prepare equipment for use.
• Execute manufacturing instructions to perform compounding, filtration, formulation, and fill activities for aseptic and terminally sterilized products in accordance with SOPs.
• Strongly adhere to verbal instructions and written procedures when operating production equipment and performing processing steps.
• Accurately complete all required production documentation, ensuring forms, logbooks, form preparations, and batch records are complete, reviewed, and meet Good Documentation Practices (GDP).
• Perform room sanitization activities to maintain controlled environment conditions.
• Identify, elevate, and document events that deviate from normal operations; participate in investigations as needed; assist in introducing new manufacturing schemes into the GMP manufacturing facility.
• Execute routine and critical operations, as well as commissioning and validation activities, as assigned.
• Support the engineering, warehouse, and facilities departments to build cross-functional skills, as required.
• Perform additional duties as assigned.

Requirements

• High School Diploma with 1-2 years of work experience in mechanically based or similar role.
• 1-2 years of professional manufacturing experience in an FDA Regulated Pharmaceutical facility preferred.
• Experience reviewing and creating controlled documents preferred.
• Experience with sterile injectable drugs preferred.
• Familiarity with formulation, filling, primary packaging, and aseptic processing preferred.
• Strong knowledge of aseptic techniques is preferred.
• Willingness to work extended shifts and a variable schedule when required.
• Excellent communication skills, verbal and written.
• Experience with MS Office/Excel tools.
• Self-motivated with the ability to complete multiple floor activities in an effective and compliant manner.
• Strong attention to detail, organizational skills, and commitment to quality.
• Proven ability to plan and prioritize complex activities.
• Strong analytical skills and mechanical aptitude to identify risks and prepare balanced decisions.
• Positive attitude and strong interpersonal skills.

Benefits

• This position is eligible for overtime, which may be required based on production demands.
• W2 Temp roles include our Medical and Sick Time benefits.

Equal Opportunity Employment Statement

PSC is committed to a policy of Equal Employment Opportunity with respect to all employees, interns, and applicants for employment. Consistent with this commitment, our policy is to comply with all applicable federal, state and local laws concerning employment discrimination. Accordingly, the Company prohibits discrimination against qualified employees, interns and applicants in all aspects of employment including, but not limited to: recruitment, interviewing, hiring (or failure or refusal to hire), evaluation, compensation, promotion, job assignment, transfer, demotion, training, leaves of absence, layoff, benefits, use of facilities, working conditions, termination and employer-sponsored activities and programs, including wellness, social and recreational programs. Employment decisions will be made without regard to an applicant’s, employee’s, or intern’s actual or perceived: race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age (40 or older), disability, genetic information, or any other status protected by law.