E&L Documentation Specialist

Merck Kgaa Burlington , NC 27215

Posted 3 months ago

Your Role:

At MilliporeSigma the E&L Documentation Specialist is responsible for supporting the Validation Project Manager team and generating technical documentation to support our external Biopharmaceutical/Pharmaceutical customers. The E&L Documentation Specialist is primarily responsible for writing and reviewing both protocols and reports related to extractables and leachables testing services. This role will also have the opportunity to actively participate in multiple global projects related to activities which support our MilliporeSigma customers.

Who You Are:

Minimum Qualifications:

  • Bachelor's degree in Chemistry, Biochemistry or related science discipline with at least 1 year of experience from Biotech/Biopharmaceutical industry

Preferred Qualifications:

  • Prior experience of QA/QC, validation, and/or similar laboratory experience is preferred

  • The ability to solve problems and develop reasoning related to test results

  • Proven organization skills

  • Excellent written and verbal communication

  • Proven record keeping abilities and computer/data skills, particularly advanced Microsoft Excel skills

  • Aptitude in laboratory skills with the ability to multitask and handle different projects/responsibilities simultaneously in a fast-paced environment

  • Ability to work in a team environment and interface with various departments/geographies

  • Experience working with customers

RSRMS

Job Requisition ID: 198723

Location: Burlington

Career Level: C - Professional (1-3 years)

Working time model: full-time

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 HR Services team at 855 444 5678 from 8:00am to 5:30pm ET Monday through Friday.


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VIEW JOBS 11/8/2019 12:00:00 AM 2020-02-06T00:00 Your Role: At MilliporeSigma the E&L Documentation Specialist is responsible for supporting the Validation Project Manager team and generating technical documentation to support our external Biopharmaceutical/Pharmaceutical customers. The E&L Documentation Specialist is primarily responsible for writing and reviewing both protocols and reports related to extractables and leachables testing services. This role will also have the opportunity to actively participate in multiple global projects related to activities which support our MilliporeSigma customers. Who You Are: Minimum Qualifications: * Bachelor's degree in Chemistry, Biochemistry or related science discipline with at least 1 year of experience from Biotech/Biopharmaceutical industry Preferred Qualifications: * Prior experience of QA/QC, validation, and/or similar laboratory experience is preferred * The ability to solve problems and develop reasoning related to test results * Proven organization skills * Excellent written and verbal communication * Proven record keeping abilities and computer/data skills, particularly advanced Microsoft Excel skills * Aptitude in laboratory skills with the ability to multitask and handle different projects/responsibilities simultaneously in a fast-paced environment * Ability to work in a team environment and interface with various departments/geographies * Experience working with customers RSRMS Job Requisition ID: 198723 Location: Burlington Career Level: C - Professional (1-3 years) Working time model: full-time 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 HR Services team at 855 444 5678 from 8:00am to 5:30pm ET Monday through Friday. Nearest Major Market: Boston Job Segment: Biochemistry, Biotech, Pharmaceutical, Laboratory, Science, Research EMD Millipore Burlington NC

E&L Documentation Specialist

Merck Kgaa