Document Control Supervisor

Job description

A career with MilliporeSigma is an ongoing journey of discovery: our 60,300 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.

 

This role does not offer sponsorship for work authorization.  External applicants must be eligible to work in the US.  

  

Your Role: 

MilliporeSigma is seeking to hire an experienced supervisor and leader for its Quality Assurance Document Control team. The Quality Assurance Document Control Supervisor, as part of the Rocklin site Quality team, is responsible for ensuring compliance with the Quality Document and Learning Management Systems released to products manufactured at the Rocklin site.  Document Control Supervisor ensures Quality Document and Learning Management Systems (Training Systems) are conducted in accordance with the Site Quality Management Systems and safety requirements and applicable regulations.  The Document Control Supervisor provides technical support to internal and external customers in the achievement of product quality.

 

·  Provide guidance and workflow support and prioritization for Document Center team members.
·  Looks for ways to improve and promote quality.
·  Supervision of Quality Documentation System processes and documentation.
·  Supervision of label and other customer facing documentation generation.
·  Ensure alignment of employee learning and training assignments within the company Learning Management System.

 

Who You Are:

Minimum Qualifications:

·  Bachelor’s Degree in Molecular Biology, Biology, Biochemistry, or other Biological Science discipline or 4+ years’ experience in a laboratory or quality role within a regulated manufacturing environment.
·  3+ years’ experience in a pharmaceutical, biotechnology, medical device or other FDA regulated industry.
·  2+ years’ leadership experience.

 

Preferred Qualifications:

·  Working knowledge of ISO13485, IVDD, and IVDR regulations and requirements.
·  Ability to manage a team and clearly communicate expectations.
·  Working knowledge of manufacturing ERP Systems (SAP).
·  Excellent verbal and written communication skills.
·  Ability to adapt to rapidly changing business circumstance and the ability to thrive in a constantly changing business environment.

 

 

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences.
We celebrate all dimensions of diversity. We believe that it drives excellence, innovation, and human progress. We care about our customers, patients, and our rich mix of people. This diversity strengthens our ability to lead in science and technology.
We are committed to creating access and opportunities for all and empower you to fulfil your ambitions. Our diverse businesses offer various career moves to seek new horizons.
Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to bring their curiosity to life!

 

If you would like to know more about what diversity, equity, and inclusion means to us, please visit https://www.emdgroup.com/en/company/press-positions.html

 

If you are a resident of Colorado or New York City, you are eligible to receive additional information about the compensation and benefits, which we will provide upon request. You may contact 855 444 5678 from 8:00am to 5:30pm ET Monday through Friday, for assistance

 

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.

 

As an employee of the Company, you will be required to comply with all of the Company’s COVID-19 safety protocols and policies. The organization has currently suspended enforcement of its COVID-19 Vaccination Policy, but that policy may be reinstated by the Company in its discretion.

Job Requisition ID:  258015

Location:  Rocklin

Career Level:  D - Professional (4-9 years)

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

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. If you are a resident of a Connecticut or Colorado, you are eligible to receive additional information about the compensation and benefits, which we will provide upon request.  You may contact 855 444 5678 from 8:00am to 5:30pm ET Monday through Friday, for assistance.

Notice on Fraudulent Job Offers
Unfortunately, we are aware of third parties that pretend to represent our company offering unauthorized employment opportunities. If you think a fraudulent source is offering you a job, please have a look at the following information .

Job Segment: Biochemistry, Biology, Biotech, Document Control, QA, Science, Administrative, Quality