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Quality Technician II, Aseptic Control (Night Shift - 12-Hour Rotating Schedule)

Resilience

West Chester (OH, Chester County)

On-site

USD 10,000 - 60,000

Full time

6 days ago
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Job summary

Join a forward-thinking company at the forefront of biomanufacturing, where your role will directly impact the future of medicine. This position offers the chance to work in a dynamic environment, ensuring compliance and quality in a sterile manufacturing setting. You'll be responsible for environmental monitoring, data entry, and maintaining meticulous records, all while collaborating with a supportive team. With a focus on innovation and sustainability, this role not only promises a rewarding career but also the opportunity to contribute to meaningful advancements in healthcare. If you're detail-oriented and passionate about making a difference, this could be the perfect fit for you.

Benefits

401(k) plan with company match
Annual cash bonus program
Medical, dental, and vision insurance
Flexible time off
Tuition reimbursement
Paid holidays
Family building benefits
Life and disability insurance

Qualifications

  • Experience in a pharmaceutical production environment is required.
  • Must effectively communicate and follow instructions in English.

Responsibilities

  • Perform environmental monitoring tasks to support regulatory requirements.
  • Maintain accurate records and complete required training.

Skills

Detail-oriented
Mathematical calculations
Communication skills

Education

B.S. in Biology
Related discipline

Tools

MODA
Microsoft applications

Job description

A career at Resilience is more than just a job - it's an opportunity to change the future.

Resilience is a technology-focused biomanufacturing company that's changing the way medicine is made. We're building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need.

For more information, please visit www.resilience.com

Position Summary & Responsibilities:

This position is responsible for autonomously performing tasks related to environmental monitoring to support regulatory requirements of a sterile manufacturing site. These activities may include, but are not limited to:

  • Perform routine sampling activities and associated data entry.

  • Wear gowning, sterile garments, and PPE (Personal Protective Equipment) as required by specific activities.

  • Read and interpret diagrams, drawings, and other schematics.

  • Prepare documentation of activities, actions, and results. Ensure proper documentation practices during job activities. Read SOPs (Standard Operating Procedures) and excerpts from technical documentation.

  • Maintain accurate and complete records (for example: laboratory notebooks, quality records, sample receipts).

  • Complete required training.

  • Perform visual inspections.

  • Use MODA to collect and analyze samples.

  • Guide others on SOPs (Standard Operating Procedures), control documents, and/or other work instructions. Coordinate activities of support groups.

  • Ensure that others carry out laboratory duties in a manner consistent with cGMP.

  • Perform regular audits of SOPs (Standard Operating Procedures) and/or work instructions.

  • Recommend and initiate activities to ensure area and equipment is maintained in a state of compliance.

  • Provide feedback on service and quality issues on a timely basis.

Hours (Night shift):

  • 6pm - 6:30pm

  • 2/2/3 (12-Hour Rotating Shift)


Minimum Qualifications:

  • Prior experience in a pharmaceutical production environment

  • Must have the ability to effectively understand, read, write, communicate, and follow instructions in the English language

  • Thorough attention to detail is required

  • Must be capable of keeping accurate records and performing mathematical calculations

Preferred Qualifications

  • B.S. in biology or other related discipline

  • Working knowledge of MODA, Microsoft applications

  • Experience working in a LEAN manufacturing environment

  • Knowledge of cGMPs and FDA policies/procedures


The items described here are representative of those that must be met successfully to perform the essential functions of this job.

Resilience is an Equal Employment Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, disability status, physical or mental disability, genetic information, or characteristic, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state, and local laws. Requests for reasonable accommodation can be made at any stage of the recruitment process.

Resilience offers employees a robust total rewards program including equity, an annual cash bonus program, a 401(k) plan with a generous company match and our benefits package which is thoughtfully designed to support our employees with great healthcare (including medical, dental and vision), family building benefits, life and disability insurance, flexible time off, paid holidays, other paid leaves of absence, tuition reimbursement and support for caregiving needs. Our target base pay hiring range for this position is $21.50 - $30.50 per hour. Actual base pay is dependent upon a number of factors, including but not limited to, the candidate's geographical location, relevant experience, qualifications, skills and knowledge. Excited about Resilience and the biomanufacturing revolution? We encourage you to apply and start a conversation with one of our recruiters.
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