Senior Manager, Quality Control Analytical

Relocation Assistance Offered

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 :

The Senior Manager, Quality Control Analytical will report to the Director of the Quality Control Analytical team at the Resilience Philadelphia site.

This motivated and organized individual with strong people skills will provide supervision and technical expertise to the QC Analytical laboratory while maintaining open communication channels to meet the needs of the organization.

She / he will work closely with the QC leadership team, Operation scheduler(s) and Manufacturing team to schedule testing and assure adherence to the QC Analytical schedule.

She / he will be responsible for timely execution, review and approval of results for in process, bulk, final product, and stability samples.

The Senior Manager, Quality Control Analytical will partner with Analytical Development to coordinate the transfer and qualification / validation of new assays in the QC Analytical Laboratory.

The Senior Manager, Quality Control Analytical will ensure that the QC Analytical laboratory is operating as expected; She / he will partner with Facilities to coordinate QC Analytical equipment and instrument maintenance and calibration.

She / he will ensure the laboratory housekeeping activities are completed to maintain the QC Analytical laboratory in a state of compliance.

The Sr. QC Analytical Manager will be accountable for the closure of complex analytical investigations.

This role may provide occasional technical and supervisory oversight on weekends and off-hour, supporting QC Analysts working during shift.

Responsibilities include, but are not limited to :

Lead, manage and develop QC Analysts team members.

Schedule and coordinate laboratory activities to support in-process, bulk, final product and stability testing to meet established Turn-Around-Time.

Assist in understanding and / or solve technical problems related to QC issues. Lead complex investigations for QC related issues, in conjunction with QC investigator.

Author, review and / or approve Deviations, CAPA and Change Controls, as assigned by QC Director.

Participate in generation, review and approvals of method qualification / validation protocols, executed protocols and reports in collaboration with Analytical Development;

Author and / or review and approve QC Test Methods, SOPs, Work Instructions and all other documentation required in accordance with quality requirements.

Identify and drive operational excellence and continuous improvement opportunities within the Resilience Philadelphia site.

Contribute to Global initiatives with the Resilience network.

Understand the requirements, expectations and needs of internal and external customers and interact in courteous, professional, supportive, and collaborative manner.

Minimum Qualifications :

Work experience in a cGMP environment

Prior supervisory experience

Experience authoring and / or reviewing Deviations, Investigations, CAPA and / or Change Control

Demonstrated ability to take ownership, initiative, and self-accountability

Demonstrated ability to collaborate, work, and communicate effectively across organizational interfaces in a fast-paced dynamic team setting

Attention to detail and quick learning / application of concepts and information

Preferred Qualifications :

BS of MS degree in Biology, Biochemistry, Molecular Biology or other relevant field

Experience in Cell or Gene Therapy preferred

Flow cytometry, qPCR / ddPCR, cell-based potency and / or ELISA experience Experience with method qualification and / or validation

This position may also include the following conditions :

All employees are expected to adhere to the Quality Management System established in the Quality Manual, Quality Policy, Standard Operating Procedures, Current Good Manufacturing Practices, and any other applicable regulations and standards to the duties within their role.

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 $120,000.00 - $180,000.00 per year. 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.