Technician I, Tech Services

About Site

Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the Harmans/BWI campus. The campus, featuring two manufacturing facilities is located 5 miles from the Baltimore Washington International (BWI) airport and 13 miles from our Baltimore location. The campus is close to Washington, DC’s I-270 Technology Corridor, top universities, and government agencies.

The Harmans/BWI-1 EMA and FDA approved facility, at approximately 200,000 sq. ft., houses 10 CGMP manufacturing suites, fill/finish, central services, testing labs, and a warehouse.

The Harmans/BWI-2 facility, at approximately 145,000 sq. ft., is under development and will house 8 CGMP manufacturing suites and cold storage warehousing.

Both facilities support Phase 3 through commercial manufacturing of advanced therapeutic products including AAV and other viral vector-based therapies and vaccines.

Position Summary

We have an opportunity for a Technician I, Tech Services to join our team. In this role, you will support GMP manufacturing by maintaining gowning inventory and ensuring the sterility of equipment and environment. You will follow all GMP standards and quality requirements, including documentation. This position reports to the Supervisor, Tech Services and plays a key role in supporting manufacturing operations.

Shift: Day shift 7am-7pm on a 2-2-3 rotation
Location: Harmans, MD - BWI
100% Onsite

The Role

Follow all Standard Operating Procedures and adhere to cGMP's and GDP's.
Ensure gowning areas into and within Manufacturing areas are constantly stocked with supplies.
Day-to-day duties include but are not limited to: Equipment Wash Room / Parts Washer, Equipment & Parts Sterilization / Autoclave, WFI Port Flushing, Filter Integrity Testing, Monitor supply inventory, Room Wash Down / Turn-over.
Perform cleaning procedures on processing equipment and manufacturing areas using written procedures, cleaning solutions, and materials.
Ensure all training is up to date on all cGMP manufacturing operations and documentation and adhering to safety guidelines .
Perform other related duties as assigned to meet departmental and Company objectives.
Other duties as assigned.

The Candidate

Minimum Requirements

High school diploma or General Education Diploma required.
0-1 years of experience working in a regulated environment preferred (will consider reduced experience with higher education in an applicable discipline).
Strong communication skills.
Must be able to lift up to 25 lbs minimum.
Basic computer skills including Microsoft Office.
Ability to work in a lean, action-oriented organization and demonstrate a strong work ethic.
Must be flexible, adaptable, self-motivated, and able to work well independently and across teams and partners.
Ability to develop and maintain strong working relationships with primary support functions.
Perform other related duties as assigned to meet departmental and company objectives.
Must be able to lift up to 25 lbs minimum.
Extended amounts of time standing, bending, and walking.

Pay

The anticipated hourly rate for this position in MD is $21.63 – $26.44 Plus Bonus. The final hourly rate offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Catalent is a multi-state employer, and this salary range may not reflect positions that work in other states.

Why You Should Join Catalent

Defined career path and annual performance review and feedback process.
Diverse, inclusive culture.
Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives.
Competitive paid time off plus 8 paid holidays.
Community engagement and green initiatives.
Medical, dental, and vision benefits effective day one of employment.
Tuition reimbursement.

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.

Catalent is an Equal Opportunity Employer, including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

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