Technician I, Central Services
Catalent Pharma Solutions is looking to hire a Technician I, Central Services (Day Shift) to support our Gene Therapy Team in Harmans, MD
This position will take place on day shift, (7:00am-7:00pm on a 2-3-2 rotation). This role will require a rotating schedule that will include working on Weekends.
The Central Services Technician I will be expected to support the execution of GMP manufacturing batch records and ensures necessary supply levels in the manufacturing areas. This role is also responsible for supporting the overall GMP 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 products from microbial and cell culture systems for GMP manufacturing. 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.
Catalent Cell & Gene Therapy is a premier development and manufacturing organization supporting the pharmaceutical and biotechnology industries. Catalent focuses on bringing client drug compounds from discovery to the clinic with services that include analytical development, pre-formulation testing, formulation development, GMP manufacturing and stability storage and testing.
At Catalent Cell & Gene Therapy, we recruit and develop exceptional individuals with a passion for science and determination to excel. We offer a technically challenging and stimulating environment and the opportunity to learn from the best.
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
Execution of manufacturing batch records, SMP's, work instructions, and/or SOPs, with minimal instruction on a day-to-day basis and a focus on proactive ‘right the first time’ executions.Documentation of all activities to meet cGMP requirements.Proven ability to utilize central services processing equipment according to established SOPs. This equipment includes but is not limited to biological safety cabinets, various mixers, autoclaves, washers, balances/scales, Ph/ Conductivity meters.Help identify and support the implementation of Continuous Improvement opportunities.Have the ability to identify Waste within work processes.Identify Cost Savings projects / InitiativesAdhere to all cGMPs, compliance/regulatory mandates, and quality requirements.Review his/her daily GMP documentation for accuracy and completeness…(Logbooks, SMP, & Batch records)Other duties as assignedThe Candidate
High school diploma or GED required1-2 years' experience working in a GMP facility preferred (will consider reduced experience with increased levels of education in applicable discipline)Strong communication skills and must have basic computer skills including Microsoft OfficeMust be able to lift up to 25lbs minimum and be able to spend extended periods of time standing and walking.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.The anticipated salary range for this position in Maryland is $39,680 - $54,560 plus shift differential 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
Potential for career growth within an expanding team.Defined career path and annual performance review & feedback process.Cross-functional exposure to other areas within the organization.Medical, Dental, Vision, and 401K are all offered from day one of employment.152 hours of PTO and 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.
personal initiative. dynamic pace. meaningful work.
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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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