Central Services Technician I - HireTalent
Harmans, MD 21077
About the Job
Job Title: Central Services Technician I
Job Location: Harmans, MD
Job Contract: TEMP TO HIRE -3 MONTHS
SHIFT 7 am 7 pm (2-2-3 rotation)
Description/Comment:
"As the Central Services Technician I, I will be expected to support the execution of GMP manufacturing batch records and ensure 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 and 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
Key Responsibilities include but are not limited to:
" Execution of manufacturing batch records, SMPs, work instructions, and 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, and 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 / Initiatives
" Adhere to all cGMPs, compliance/regulatory mandates, and quality requirements.
" Review his/her daily GMP documentation for accuracy and completeness...(Logbooks, SMP, & Batch records)
Education & Experience:
" High school diploma or GED required
" 1-2 years experience working in a GMP facility preferred (will consider reduced experience with increased levels of education in applicable discipline)
" Strong communication skills
" Must be able to lift to 25lbs 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.
" Perform other related duties as assigned to meet departmental and Company objectives.
" Ability to develop and maintain strong working relationships with primary support functions.
Job Location: Harmans, MD
Job Contract: TEMP TO HIRE -3 MONTHS
SHIFT 7 am 7 pm (2-2-3 rotation)
Description/Comment:
"As the Central Services Technician I, I will be expected to support the execution of GMP manufacturing batch records and ensure 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 and 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
Key Responsibilities include but are not limited to:
" Execution of manufacturing batch records, SMPs, work instructions, and 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, and 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 / Initiatives
" Adhere to all cGMPs, compliance/regulatory mandates, and quality requirements.
" Review his/her daily GMP documentation for accuracy and completeness...(Logbooks, SMP, & Batch records)
Education & Experience:
" High school diploma or GED required
" 1-2 years experience working in a GMP facility preferred (will consider reduced experience with increased levels of education in applicable discipline)
" Strong communication skills
" Must be able to lift to 25lbs 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.
" Perform other related duties as assigned to meet departmental and Company objectives.
" Ability to develop and maintain strong working relationships with primary support functions.
Source : HireTalent