Catalent hires people with a passion to make a difference to the
health of millions of people globally. Your expertise, coupled with
Catalent's advanced technologies and collaboration with thousands
of innovative pharmaceutical, biotech and healthcare companies,
will help bring life-enhancing products to the people you know and
love. Your talents, ideas and passion are essential to our mission;
to develop, manufacture and supply products that help people live
better, healthier lives. Interested in learning more about life at
Catalent? Start here
We are hiring a Manufacturing Associate I to join our growing
Manufacturing Team at our Montgomery facility.
The Manufacturing Associate I is responsible for supporting the
overall GMP downstream manufacturing process, through the
application of broad knowledge of theories and principles utilized
to solve operational, as well as routine tasks in the production of
bulk biologics from microbial and cell culture systems for Phase
I/II & commercial GMP manufacturing.
The Manufacturing Associate I role is critical to our patients.
Manufacturing life-saving medicines right the first time for
themselves and their team with patient safety in mind is our
priority. Quality, safety and on-time delivery is a must to be
successful in this role!
- Performs Processing Steps and/or Manufacturing Support
activities, monitoring process against the batch record.
- Documents/Records cGMP data and information for processing
steps and/or equipment activities, following standard operating
procedures. Key documentation includes batch records and equipment
- Performs the weighing, dispensing of raw materials for media
- Performs the preparation of small and large volume media and
buffer solutions, filtration and transfer of product.
- Operates bench top equipment including pH, conductivity, osmo
meters, pumps, tubing welders, filter integrity testers etc.
- Dispensing, labeling, transfer/staging of raw materials and
- Maintaining equipment, area and cleaning logbooks
- May author/ review/improve SOP's, batch records, protocols and
- High School Diploma with a minimum of 2-4 years GMP
Manufacturing experience, OR
- Associate's Degree in a scientific, engineering or
biotechnology discipline with a minimum of 0-2 years related
experience; coursework with biotechnology focus highly desirable,
- Bachelor's Degree (BS/BA) from an accredited college or
university with an emphasis in a scientific or engineering
discipline and a minimum of 0-1 years relevant experience
We will identify candidates based on the following:
- Leads with Integrity and Respect
- Delivers Results
- Demonstrates Business Acumen
- Fosters Collaboration and Teamwork
- Champions Change
- Engages and Inspires
- Coaches and Develops
- Join a high growth and fast paced organization with a people
- Global exposure, defined career path and annual performance
review and feedback process
- Cross functional exposure to other areas of within the
- Medical, Dental, Vision, and 401K are all offered from day one
- 19 days of paid time off annually + 8 paid holidays
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.
Catalent is committed to the health and safety of its employees,
visitors and the customers and patients we serve. As a result of
the global pandemic, we have modified many of our recruitment and
on-boarding processes to maintain everyone's safety. The Human
Resources teams will communicate all necessary safety processes and
procedures throughout each stage.
personal initiative. dynamic pace. meaningful work.
Visit www.catalent.com/careers to explore career
Catalent is an Equal Opportunity / Affirmative Action employer.
All qualified applicants will receive consideration for employment
without regard to race, color, religion, sex, national origin,
disability, protected veteran status, sexual orientation or gender
identity. 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.