Sr. Quality Control Microbiology Technician

Yoh, A Day & Zimmermann Company; Noblesville (IN); On-site; Full time

Job summary

A leading company is hiring a Sr. Quality Control Microbiology Technician in Noblesville, Indiana. This role involves performing quality control activities, ensuring compliance with regulatory standards, and collaborating with team members. The position requires strong analytical and problem-solving skills, along with a commitment to quality and safety in a cGMP regulated environment.

Qualifications

• 5 or more years of relevant experience required.
• General quality / production experience in a cGMP regulated facility is required.

Responsibilities

• Perform quality control activities within the Microbiology Department.
• Ensure compliance with regulatory agencies and guidelines.
• Collaborate with team members to complete testing and tasks.

Skills

Analytical

Problem Solving

Attention to Detail

Interpersonal Skills

Communication

Education

Associate Degree

Job description

Sr. Quality Control Microbiology Technician

Sr. Quality Control Microbiology Technician

4 days ago Be among the first 25 applicants

Direct message the job poster from Yoh, A Day & Zimmermann Company

Principal Scientific Recruiter at Yoh, A Day & Zimmermann Company

Yoh is hiring a for a QC Microbiologist Technician for our Pharmaceutical client in Noblesville, Indiana. This a contract opportunity to join a growing team.

Summary of Position Perform assigned quality control activities within the Microbiology Department to comply with applicable SOP's and cGMPs. Work under limited supervision with considerable latitude for the use of initiative and independent judgment. Must have the ability to work collaboratively, multitask, and adapt to changing priorities and schedules.

Schedule: Monday - Friday 8am - 4:30pm

Essential Functions

• Must maintain operational compliance with US and international regulatory agencies and guidelines (i.e. FDA, EU, HC, TGA, PIC/S, ISO, USP, NRC, cGMP, etc.).
• Employ aseptic techniques while performing Sterility, Endotoxin, Particulates and Bioburden testing of drug products, intermediates and raw materials per USP and Curium Standard Operating Procedures (SOP)
• Perform in vivo biological performance testing of final product in support of product efficacy and quality per USP and Curium Standard Test Methods
• Perform Growth Promotion testing per USP Methods for various microbiological media.
• Prepare and analyze Biological Indicators in support of Validation and Qualification activities.
• Read plates to quantify microbial growth and subculture pure isolates as required.
• Data entry and review in Laboratory Management Systems (LIMS).
• General laboratory housekeeping duties and maintenance of the department, premises, and equipment.
• Collaborate with other team members to ensure the consistent and timely completion of all testing and other tasks in support of business needs.
• Assist with laboratory investigations, root cause analysis, and implementation of corrective and preventative actions.
• Ensure a safe and quality-minded working environment through conformance with training, general awareness, and compliance to safety/Quality guidelines and SOPs.
• Perform all work in compliance with site safety and radiation protection guidelines.
• Attend mandatory trainings as required by site regulatory requirements and management.
• Perform other general duties associated with the position as required by supervision.
• Management of inventory and ensuring all laboratory supplies are appropriately stocked.
• Assist in monthly equipment safety inspections.
• Assist in the training of less experienced technicians.
• Perform alert recovery trending.

Education/Experience Requirements

• Associate Degree or completion of 4 college-level life science courses required. Work experience is considered in lieu of degree.
• 5 or more years of relevant experience required.
• Willingness to perform in vivo testing in support of product efficacy and quality.
• General quality / production experience in a cGMP regulated facility is required.
• Good interpersonal skills, good hands on, analytical, problem solving and decision-making skills.
• Excellent writing and verbal communications skills
• Close attention to detail required.
• Good computer skills, including utilizing personal computers and data entry programs.
• Ability to work independently and with others to accomplish goals and priorities.
• Flexibility and teamwork skills.
• High level of energy and regular, consistent attendance.
  

Estimated Min Rate: $25.00
Estimated Max Rate: $30.00

Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.

Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Visithttps://www.yoh.com/applicants-with-disabilitiesto contact us if you are an individual with a disability and require accommodation in the application process.

For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Contract

Job function

• Job function

  Research and Science

• Industries

  Pharmaceutical Manufacturing

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