Supervisor, QC Chemistry

at  Emergent BioSolutions

Winnipeg, MB, Canada -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate19 Jan, 2025Not Specified19 Oct, 20245 year(s) or aboveModeling,Gmp,Communication Skills,Career Opportunities,Select Agents,Disabilities,Design,WhmisNoNo
Add to Wishlist Apply All Jobs
Required Visa Status:
CitizenGC
US CitizenStudent Visa
H1BCPT
OPTH4 Spouse of H1B
GC Green Card
Employment Type:
Full TimePart Time
PermanentIndependent - 1099
Contract – W2C2H Independent
C2H W2Contract – Corp 2 Corp
Contract to Hire – Corp 2 Corp

Description:

Those who join Emergent BioSolutions feel a sense of ownership about their future. You will excel in an environment characterized by respect, innovation and growth opportunities. Here, you will join passionate professionals who advance their scientific, technical and professional skills to develop products designed-to protect life.
Job Summary
The Supervisor of Quality Control provides immediate supervision to a group of Quality Control employees in their successful execution of key quality responsibilities and assigned tasks, and checks work at frequent intervals to ensure that Quality Control objectives and accountabilities are met. A portion of time is normally spent performing individual tasks related to the unit. The Supervisor also serves as a resource of technical knowledge for established assays and exercises judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions.
Responsibilies

Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions.

  • Accountable for planning, scheduling, allocating, and the prioritizing of the workload to meet operating requirements in the assigned Quality Control area.
  • May lead some laboratory investigations and provides oversight to the content of investigation reports.
  • Uses analytical data and/or statistical concepts such as SPC, regression analysis, and product and material trends to understand variables impacting assay and process performance. Investigates aberrant trends and assists with troubleshooting of test procedures.
  • Ensures adherence to quality standards and ensures compliance with the requirements of current Good Manufacturing Practices (cGMP).
  • Applies expertise to support change and risk management, including application of scientific and technical innovation.
  • Initiates or coordinates the preparation of reports and maintenance of records pertaining to the operation of the work unit in a manner suitable for regulatory submission or inspection. Ensures the reliability and accuracy of the computer databases and paper files.
  • Coordinates/leads cross-functional teams in process mapping and other exercises designed to facilitate process and system understanding. Initiates and coordinates complex projects with other departments and interacts with other department personnel to accomplish objectives.
  • Coaches employees through problems of diverse scope in which analysis of situations or data requires evaluation of identifiable factors. Directs subordinates to complete assignments using established guidelines, procedures and policies.
  • Coaches employees in the areas of performance and provides routine guidance and performance feedback. Act as an advisor to the unit and resolve problems to meet business objectives.
  • Provide development opportunities to staff through training, development plans, participation in appropriately challenging activities and applying leadership architect concepts.
  • Work in collaboration with direct manager, subordinates, internal customers and other cross functional peers to gain alignment on sound quality decisions.
  • Support workforce diversity, safety and adherence to company core values.
  • The ability to work days, evening or nights may be required.

Education, Experience & Skills

  • Minimum of 5 years of relevant experience, accompanied by a bachelor’s degree in science, or an equivalent combination of education and experience.
  • Requires a broad scope of technical knowledge to assist with modeling or design, complex troubleshooting, draft method validation protocols, and/or investigate complex deviations.
  • Excellent written and verbal communication skills.
  • Thorough knowledge of GMP and WHMIS and biohazard safety awareness.
  • Scientific knowledge of standard practices in area of assignment.
  • Knowledge of supervisory practices and techniques.
  • Ability to conduct investigative interviews.
  • A pre-employement an annual medical is required for this role.

Responsibilities:

  • Accountable for planning, scheduling, allocating, and the prioritizing of the workload to meet operating requirements in the assigned Quality Control area.
  • May lead some laboratory investigations and provides oversight to the content of investigation reports.
  • Uses analytical data and/or statistical concepts such as SPC, regression analysis, and product and material trends to understand variables impacting assay and process performance. Investigates aberrant trends and assists with troubleshooting of test procedures.
  • Ensures adherence to quality standards and ensures compliance with the requirements of current Good Manufacturing Practices (cGMP).
  • Applies expertise to support change and risk management, including application of scientific and technical innovation.
  • Initiates or coordinates the preparation of reports and maintenance of records pertaining to the operation of the work unit in a manner suitable for regulatory submission or inspection. Ensures the reliability and accuracy of the computer databases and paper files.
  • Coordinates/leads cross-functional teams in process mapping and other exercises designed to facilitate process and system understanding. Initiates and coordinates complex projects with other departments and interacts with other department personnel to accomplish objectives.
  • Coaches employees through problems of diverse scope in which analysis of situations or data requires evaluation of identifiable factors. Directs subordinates to complete assignments using established guidelines, procedures and policies.
  • Coaches employees in the areas of performance and provides routine guidance and performance feedback. Act as an advisor to the unit and resolve problems to meet business objectives.
  • Provide development opportunities to staff through training, development plans, participation in appropriately challenging activities and applying leadership architect concepts.
  • Work in collaboration with direct manager, subordinates, internal customers and other cross functional peers to gain alignment on sound quality decisions.
  • Support workforce diversity, safety and adherence to company core values.
  • The ability to work days, evening or nights may be required


REQUIREMENT SUMMARY

Min:5.0Max:10.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Science or an equivalent combination of education and experience

Proficient

1

Winnipeg, MB, Canada