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Manufacturing Supervisor (Entry Level)
New Brunswick, New Jersey · Biotech/PharmaceuticalAre you looking to be a part of a growing pharmaceutical company? One of our largest clients is currently seeking a Manufacturing Supervisor (Entry Level) to join their New Brunswick, New Jersey team. Our client is one of the leading pharmaceutical companies specializing in developing and manufacturing solid dosage products. If you believe you are qualified, we would be excited to connect and discuss this opportunity in more detail.
Please visit us at https://www.prostaffworkforce.com/ to explore all opportunities.
Direct Hire
1st shift
Pay Rate: (Will depend on Experience)
Job Summary:
The Manufacturing Supervisor assumes a critical role in performing and managing the Production Operations in manufacturing facility. Must manage and document, manufacturing / packaging operations as per cGMP / SOP and BMR requirements. Manages Team Leads and Operators on a daily basis. Conducts periodic checks on documents and take corrective actions to prevent deviations. Ensures target production numbers are met on a daily basis and cGMP documents are completed in a timely manner. Plays an active role for adherence to GMP and safety.
Responsibilities:
· Based on the production planning, coordinates and supervises the daily/weekly manufacturing activities of production staff in assigned areas.
· Coordinates work activities with other supervisors and sets priorities for the team to ensure task completion.
· Prepares and trains employees on manufacturing related SOPs.
· Ensures processes and procedures are followed as per batch records, SOPs, and protocols and the quality specification are met.
· Oversees scale-up, Exhibit, Characterization and validation batch execution as well as the execution of cleaning verification /validation protocols.
· Initiates any event/investigations and change controls.
· Applies expertise to solve standard and non-standard problems within the manufacturing area.
· Works within budgetary/ financial objectives, applying knowledge of profit drivers to work processes.
· Resolves day-to-day or routine manufacturing problems using defined processes.
· Works/brainstorms with work team and provides suggestions for solutions that contain the appropriate level of risk; ensures work team understands and supports the focus on operational excellence.
· Effectively builds alignment on difficult issues.
· Follows the DEA Controlled Substance SOPs and reports any violation to Manager.
Qualifications:
· Bachelor degree in Engineering (any discipline) or Pharmaceutical or Pharmacology
· Minimum of 1-2 years of manufacturing experience required.
· Knowledge of granulation, blending/mixing, compression (AWC machines), coating, encapsulation equipment
· Able to work extended hour to achieve manufacturing schedule when required.
· Builds confidence and respect of others through a positive and energizing style
· Demonstrated proficiency with MS Office applications.
· Ability to work under pressure and meet tight deadlines.
· Good problem solving and decision making skills.
· Sound knowledge of cGMP's, SOP's, FDA guidelines and safety regulations
· Demonstrated excellent communication: verbal, written and presentation skills.
· A self-starter with a hands-on approach and a can-do attitude. .
· The requirement for English language proficiency for this job role is IntermediateB1+ (comparable to Global CEFR Independent B1) level based on the Common European Framework of Reference for Languages (CEFR).
Our client offers a competitive compensation package as well as an excellent benefits package for eligible candidates.
#IND2
Please visit us at https://www.prostaffworkforce.com/ to explore all opportunities.
Direct Hire
1st shift
Pay Rate: (Will depend on Experience)
Job Summary:
The Manufacturing Supervisor assumes a critical role in performing and managing the Production Operations in manufacturing facility. Must manage and document, manufacturing / packaging operations as per cGMP / SOP and BMR requirements. Manages Team Leads and Operators on a daily basis. Conducts periodic checks on documents and take corrective actions to prevent deviations. Ensures target production numbers are met on a daily basis and cGMP documents are completed in a timely manner. Plays an active role for adherence to GMP and safety.
Responsibilities:
· Based on the production planning, coordinates and supervises the daily/weekly manufacturing activities of production staff in assigned areas.
· Coordinates work activities with other supervisors and sets priorities for the team to ensure task completion.
· Prepares and trains employees on manufacturing related SOPs.
· Ensures processes and procedures are followed as per batch records, SOPs, and protocols and the quality specification are met.
· Oversees scale-up, Exhibit, Characterization and validation batch execution as well as the execution of cleaning verification /validation protocols.
· Initiates any event/investigations and change controls.
· Applies expertise to solve standard and non-standard problems within the manufacturing area.
· Works within budgetary/ financial objectives, applying knowledge of profit drivers to work processes.
· Resolves day-to-day or routine manufacturing problems using defined processes.
· Works/brainstorms with work team and provides suggestions for solutions that contain the appropriate level of risk; ensures work team understands and supports the focus on operational excellence.
· Effectively builds alignment on difficult issues.
· Follows the DEA Controlled Substance SOPs and reports any violation to Manager.
Qualifications:
· Bachelor degree in Engineering (any discipline) or Pharmaceutical or Pharmacology
· Minimum of 1-2 years of manufacturing experience required.
· Knowledge of granulation, blending/mixing, compression (AWC machines), coating, encapsulation equipment
· Able to work extended hour to achieve manufacturing schedule when required.
· Builds confidence and respect of others through a positive and energizing style
· Demonstrated proficiency with MS Office applications.
· Ability to work under pressure and meet tight deadlines.
· Good problem solving and decision making skills.
· Sound knowledge of cGMP's, SOP's, FDA guidelines and safety regulations
· Demonstrated excellent communication: verbal, written and presentation skills.
· A self-starter with a hands-on approach and a can-do attitude. .
· The requirement for English language proficiency for this job role is IntermediateB1+ (comparable to Global CEFR Independent B1) level based on the Common European Framework of Reference for Languages (CEFR).
Our client offers a competitive compensation package as well as an excellent benefits package for eligible candidates.
#IND2