Offers “Merckgroup”

Expires soon Merckgroup

Manufacturing Supervisor

  • Carlsbad (San Diego)
  • Accounting / Management control

Job description

A career with MilliporeSigma is an ongoing journey of discovery: our 58,000 people are shaping how the world lives, works and plays through next generation advancements in Healthcare, Life Science and Electronics. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others. MilliporeSigma is a business of Merck KGaA, Darmstadt, Germany.    

 

Your Role:

The Manufacturing Supervisor will demonstrate a high level of competency and knowhow related to all aspects of technical cGMP biopharmaceutical buffer and media manufacturing. The Supervisor of MFF is also responsible for cGMP drug substance and drug product filling operations within a cGMP production facility.

·  Guide projects and team leaders to ensure production projects are efficient, accurate, compliant, and the associated operators have the skill levels that match the related work.
·  Responsible for leading the manufacturing staff working in the facility to meet corporate production goals, as well as influencing related, cross-functional groups to meet these objectives. 
·  Ensure the facility and equipment is maintained in a cGMP compliant state and ready for use. 
·  The employee must be able to work off-shifts, weekends, and additional hours as required.
·  The employee must have the ability to perform very complex tasks with attention to detail.
·  Ensure that the manufacturing facility operates according to cGMP regulations.
·  Maintain operations within contracted guidelines in order to successfully produce high quality bulk and finished products.
·  Build and maintain a staff that is both technically qualified and well trained in cGMP manufacturing, while providing a motivating environment and opportunities for their professional advancement in a safety conscious environment.
·  Define, implement and optimize the manufacturing schedules.
·  Ensure consistent product quality through appropriate manufacturing programs and by working with other groups such as Quality Control and Quality Assurance.
·  Lead process trouble-shooting efforts.
·  Develop, implement and update all production SOPs, Batch Records and other documentation needed for GMP production projects.
·  Ensure that deviation reports are written accurately and appropriately as they occur. Track and implement corrective actions.
·  Provide a safe working environment for employees.
·  Evaluate employee efficiency and productivity.
·  Spend 50% or more of time on work directly and closely related to carrying out exempt functions.
·  Spend approximately 25% of time working in the facility, training and assisting the Technicians and Biologists.
·  Well-honed priority and time management skills.

 

 

Who you are:

Minimum Qualifications:

·  Bachelor of Science degree in Chemistry, Biology or other Health Care indication
·  8+ years of experience in Manufacturing Upstream and/or Downstream
·  4+ years of team leadership experience in a GMP environment
·  4+ years of experience in and with aseptic manufacturing processes
·  2+ years of direct people management

 

Preferred Qualifications:

·  Lean Six Sigma methodologies experience preferred
·  Excellent written and verbal communication skills
·  Knowledge of relevant unit operations and trouble shooting experience as a supervisor
·  Experience in Bulk Drug UF/DF Formulation and sterile Filtration
·  Working knowledge of desktop computers and technical equipment

RSRMS

 

 

 

What we offer: With us, there are always opportunities to break new ground. We empower you to fulfil your ambitions, and our diverse businesses offer various career moves to seek new horizons. We trust you with responsibility early on and support you to draw your own career map that is responsive to your aspirations and priorities in life. Join us and bring your curiosity to life!

 

Curious? Apply and find more information at https://jobs.vibrantm.com

 

The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law.  This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.

 

Job Requisition ID:  225127

Location:  Carlsbad

Career Level:  E - Professional (10+ years)

Working time model:  full-time .buttontextf748fab0b60d052d a{ border: 1px solid transparent; } .buttontextf748fab0b60d052d a:focus{ border: 1px dashed #eb3c96 !important; outline: none !important; }

Careers during Covid-19
Thank you for visiting our careers website, we are always looking for curious minds to join our teams. We understand how much the world is being impacted by the Covid-19 crisis and we want to assure you that your safety is very important to us. To ensure that everyone’s health is protected, instead of a standard face-to-face interview, it is likely that you will be offered alternative digital interview options.

US Disclosure
The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law.  This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.

North America Disclosure
The Company is committed to accessibility in its workplaces, including during the job application process. Applicants who may require accommodation during the application process should speak with our Candidate Services team at 844-655-6466 from 8:00am to 5:30pm ET Monday through Friday.

Job Segment: Manager, Lean Six Sigma, Quality Assurance, QA, QC, Management, Technology, Quality

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