Group Lead - Central Services
Company: Disability Solutions
Location: Severn
Posted on: November 10, 2024
Job Description:
Group Lead, Central Services Catalent Pharma Solutions is
looking to hire a Group Lead, Central Services (Day Shift) to
support our Gene Therapy Team in Baltimore, MD.Our Gene Therapy
facility, located at the University of Maryland (UMD) BioPark in
the city of Baltimore, MD, specializes in upstream and downstream
process development of viral vectors for clinical applications.
Baltimore is a hub of national and international travel and
communications and is also home to and near major universities and
several federal agencies, including the FDA, USDA, NIH, Johns
Hopkins University, and UMD Schools of Medicine.The facility houses
process development labs and CGMP cleanroom suites for Phase 1 and
2 programs focused on a variety of transformative technologies,
including AAV and other viral vectors, vaccines, and oncolytic
immunotherapies.The Central Services (CS) department is responsible
for the execution of clinical and commercial standard manufacturing
process (SMP). The buffers and media prepped by CS are used for
solution preparation, master/working cell bank production, upstream
cell culture and viral vector production, downstream purification,
and fill/finish operations. Further, manufacturing operations is
tasked to utilize continuous improvement methodologies to realize
process optimization, efficiency gains, and waste reduction to
maximize capacity outputs.The Central Services Group Lead is a
working lead responsible for daily execution of the operations
schedule to deliver the desired output in a safe, compliant, and
efficient manner.-- The Group Lead has broad knowledge of solution
preparation theories and principles, demonstrates systematic
problem-solving skills, and integrates continuous improvement into
the larger manufacturing organization guided by The Catalent
Way.--This position will take place on the day shift, Monday -
Friday, 8am-5pm. Catalent is committed to a Patient First culture
through excellence in quality and--compliance, and to the safety of
every patient, consumer, and Catalent employee.--The Role
- Performs daily production activities to ensure schedule
adherence.
- Coordinates, with indirect supervisory responsibilities,
production activities for a group of Manufacturing Associates /
Technicians.
- Practices operational excellence methodologies in The Catalent
Way and acts as a change agent for continuous improvement
efforts.
- Leads tier 1 meetings in the review and execution of people,
safety, quality, delivery, and cost objectives. .
- Ensure staff are fully trained on all cGMP manufacturing
operations and documentation and adhering to safety guidelines and
assists the supervisor with rapid response and problem resolution
for daily issues.
- Completes SMPs under cGMP, and documents in detail using SOPs
and SMPs for the processes and manufacturing steps. Generate and
revise internal and external documents (SOPs, SMPs).
- Support initiation and closure of deviations; may serve as the
lead in the departmental investigation and be responsible for
closing out deviations and CAPAs.
- Troubleshoot process and equipment problems; Work with
Facilities and Validation to maintain manufacturing equipment.
Recommend equipment and other supply purchases within the
production areas.
- Work closely with production management for current and new
manufacturing projects and help develop processes/techniques to
meet contract objectives and avoid operational delays. May work
with Process Development team and collaborate with Manufacturing
Sciences and Technology group to transfer new projects into GMP
production.
- Interact with clients during initial and subsequent
manufacturing campaigns; may be responsible to oversee and escort
the person-in-plant (PIP) during manufacturing campaigns.
- Participate in facility expansion and equipment validation
activities.
- Other duties as assignedThe Candidate
- Bachelor's or Master's degree in technical discipline (e.g.,
biology, biotechnology, engineering) or related life science field
with minimum of 2 years' related experience OR
- Associate's degree in technical discipline (e.g., biology,
biotechnology, engineering) or related life science field with
minimum of 4 years' related experience OR
- High School Diploma with minimum of 6 years' related
experience.
- Experience with upstream (fermentation/bioreactor) or
downstream (column chromatography, buffer/media skid) biologic
production processes under GMP compliance required.
- Thorough knowledge of current Good Manufacturing Practices
(cGMP's), and all relevant safety procedures. General understanding
of most areas in Manufacturing and supporting functional
groups.--
- Thorough understanding of quality systems in a regulated
environment and fully committed to right first time (RFT)
execution. Outstanding knowledge, and ability to apply scientific
principles utilized to solve operational, as well as routine
production tasks.
- Excellent documentation skills including comprehension, review
& establishing SMPs, or Batch Production Records, SOP's, deviation
& summary reports required.
- Must have the ability to work an available set shift; there
will be times when overtime is required.The anticipated salary
range for this position in Maryland is $75,000 to $100,000 and
annual bonus, when eligible.-- The final salary 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
- Potential for career growth on an expanding team within an
organization dedicated to preserving and bettering lives
- 152 hours of paid time off annually + 8 paid holidays
- Competitive salary with yearly bonus potential
- Community engagement and green initiatives
- Generous 401K match and Paid Time Off accrual
- Medical, dental and vision benefits effective day one of
employment
- Tuition ReimbursementCatalent 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 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 . 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.Important Security Notice
to U.S. Job Seekers:Catalent NEVER asks candidates to provide any
type of payment, bank details, photocopies of identification,
social security number or other highly sensitive personal
information during the offer process, and we NEVER do so via email
or social media. If you receive any such request, DO NOT respond-
it is a fraudulent request. Please forward such requests to
spam@catalent.com for us to investigate with local
authorities.California Job Seekers can find our California Job
Applicant Notice .
Keywords: Disability Solutions, Potomac , Group Lead - Central Services, Other , Severn, Maryland
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