drjobs Lead Associate 2 QC Microbiology Wednesday - Saturday 7am - 5pm

Lead Associate 2 QC Microbiology Wednesday - Saturday 7am - 5pm

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1 Vacancy
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Job Location drjobs

Durham County, NC - USA

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Position Overview

The Lead Associate 2 Quality Control (QC) Microbiology oversees and guides the critical operational functions of the QC Microbiology laboratory. This position holds the responsibility for conducting microbiological assays as well as effectively trains junior analysts in these areas. The role is pivotal in guaranteeing right the first time to support timely batch disposition of manufacturing goods. Additionally this role ensures technical issues are promptly escalated to laboratory management and upholds high standards of accuracy and efficiency within the laboratory operations.

Company Overview

We are Advancing tomorrows medicines and making a real difference to the world in which we live. At FUJIFILM Diosynth Biotechnologies we partner with our clients to deliver recombinant proteins viral vaccines and gene therapies to patients. As a Contract Development & Manufacturing Organization (CDMO) our focus is to combine technical leadership in cell culture microbial fermentation and viral vectors with world class GMP manufacturing facilities to advance tomorrows medicines. We seek candidates with proven ability to work independently and collaboratively to achieve optimized strategies and programs with the ultimate goal of delivering products that transform the lives of patients.

Job Description

Principal Accountabilities:

  • Performs complex microbiological testing (e.g. Bioburden Endotoxin Culture Purity and Microbial Identifications) per department Standard Operating Procedures (SOPs) and test methods for samples associated manufactured batches
  • Reviews technical data authors routine and periodic laboratory reports (e.g. Environmental Monitoring (EM) trend reports) and contributes to technical documentation and assessments
  • Supports client audits and regulatory inspections as an assay or method Subject Matter Expert (SME)
  • Ensures laboratory maintains inspection readiness data integrity and Current Good Manufacturing Practice (CGMP) compliance
  • Partners with management for technical services such as initiating events (e.g. deviations and nonconformances) within quality systems
  • Leads laboratory deviations and investigations
  • Identifies problems recommends and implements solutions while consulting with management
  • Leads and participates in project developments from concept through ensuring alignment with organizational goals
  • Partners with laboratory management to schedule daily weekly and nonroutine testing and tasks
  • Provides technical guidance and mentorship to junior associates
  • Participates in laboratory equipment qualification and validation activities
  • Troubleshoots laboratory equipment assay and method issues with the support of laboratory management
  • Performs other duties as assigned

Minimum Education and Experience Required:

  • Associate degree in Life Science Pharmaceutical or related field with 6 years of laboratory experience in a CGMP environment; or
  • Bachelors degree in Life Science Pharmaceutical or related field with 4 years of experience in a CGMP environment
  • Experience with data management systems (e.g. LIMS TrackWise)

Preferred Education and Experience:

  • 6 years of experience in a cGMP Microbiology laboratory

Knowledge Skills and Abilities:

  • Advanced knowledge of aseptic techniques and behaviors
  • Effective communication both written and verbal
  • Advanced technical writing and problemsolving skills
  • Ability to complete work independently and with minimal supervision
  • Ability to prioritize and organize work to deliver assignments according to established schedules and deadlines
  • Ability to effectively collaborate with coworkers and internal clients
  • Indepth understanding and knowledge of United States Pharmacopeia and European Pharmacopeia
  • Ability to support audit readiness for the laboratory
  • Ability to incorporate lean lab and six sigma principles into the work environment
  • Ability to manage and complete tasks according to a structured plan
  • Expertise with data management systems such as TrackWise LIMS and capability to learn basic use and navigation within the systems
  • Must be flexible to support 24/7 manufacturing facility

PHYSICAL REQUIREMENTS


PHYSICAL DEMANDS:
Will work in environment which may necessitate respiratory protection. X No Yes
May work in Mechanical/Production spaces that may require hearing protection and enrollment in a hearing conservation program. X No Yes
Will work in environment operating a motor vehicle or Powered Industrial Truck. X No Yes
Ability to discern audible cues. X No Yes
Ability to inspect or perform a task with 20/20 corrected vision visual acuity including distinguishing color. X No Yes


WORKING ENVIRONMENT


PHYSICAL DEMANDS:
Ability to ascend or descend ladders scaffolding ramps etc. X No Yes
Ability to stand for prolonged periods of time. No X Yes 60120 minutes (If yes may specify frequency/duration: up tominutes)
Ability to sit for prolonged periods of time. No X Yes 60120 minutes (If yes may specify frequency/duration: up tominutes)
Ability to conduct activities using repetitive motions that include wrists hands and/or fingers. No X Yes
Ability to operate machinery and/or power tools. No X Yes
Ability to conduct work that includes moving objects up to X pounds. No X Yes If yes X 10 lbs. 33 lbs.
Ability to bend push or pull reach to retrieve materials from 18 to 60 in height and use twisting motions. No X Yes ENVIRONMENTAL CONDITIONS
Will work in warm/cold environments. No X Yes 28C Range (If yes specify approximate temperature ranges.
Will work in outdoor elements such as precipitation and wind. X No Yes
Will work in small and/or enclosed spaces. X No Yes
Will work in heights greater than 4 feet. X No Yes

EEO Information

Fujifilm is committedto providing equal opportunities in hiring promotion and advancement compensation benefits and training regardless of nationality age gender sexual orientation or gender identity race ethnicity religion political creed ideology national or social origin disability veteran status etc.

ADA Information

If you require reasonable accommodation in completing this application interviewing completing any preemployment testing or otherwise participating in the employee selection process please direct your inquiries to our HR Department .


Required Experience:

IC

Employment Type

Unclear

Company Industry

Department / Functional Area

Quality Control

About Company

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