Introduce yourself

We'll guide you from there!

Way to kick of your application with the best life sciences recruitment partner you’ll meet!

Act fast—this position won't stay open for long!
Quality Analyst II, Quality Control Molecular Biology - Woburn, MA Woburn , MA
ID: 25665

Orbis Clinical is seeking an Analyst II, Quality Control Molecular Biology located in Woburn, MA for up until the end of the year.

Job Title: Analyst II, Quality Control Molecular Biology

Location: Woburn, MA

Contract: Up until the end of the year

Summary

This position is in the Gene Therapy Quality Control Molecular Biology group. The QC Analyst II will perform analytical methods including but not limited GC titer determination by ddPCR and qPCR, impurity testing, and other methods as needed to support in-process, drug substance and drug product release, stability to support AAV-based gene therapy programs. They will work cross-functionally with team members within Quality Control and internal stakeholders across Analytical Development and Quality Assurance. Routine work includes release and stability testing, critical reagent qualification, method validation and transfer, critical reagent qualification, analyzing data, and authoring technical documents.

Responsibilities

  • Performs routine QC testing including but not limited to: ddPCR, dPCR, and qPCR test methods in support of in-process, release, and stability.
  • Review and approval of cGMP analytical data for release and stability testing from interna and external analytical test methods  
  • Supports QC Molecular Biology laboratory operations (ex. Instrument qualification and maintenance. Housekeeping, qualify critical reagents, etc). 
  • Author and support quality events; Change controls, Deviation, CAPA, OOS Investigation, as needed. 
  • Write, prepare, and present technical data, technical reports, and standard operating procedures (SOPs), Method transfer/ validation protocol, Method transfer/ validation report for internal and external methods.  
  • Support method transfer and validation activities for development, technical transfer, and validation of late-stage assays for AAV-based gene therapy programs.
  • Author analytical method performance trend reports, as needed.
  • Work with cross functional teams with both internal and external stakeholders

Requirements

  • Experience working in the cGMP QC lab of the pharmaceutical or biopharmaceutical industry is a must. 
  • BS or MS in Biochemistry, Biology, Chemistry or a related discipline with 2+ years (BS/MS) relevant industry experience
  • Hands-on experience with performing dPCR, ddPCR and/or qPCR test method execution required.
  • Strong collaboration and team-working skills. 
  • Strong communication, interpersonal and organizational skills. 
  • Proven ability to work independently and effectively plan and organize work activities and prioritize task completion to meet schedules and deadlines. 
  • Should be highly motivated, demonstrate good technical skills, have excellent organizational and communication skills, and be able to multitask in a fast-paced environment with changing priorities. 

Physical Demand Requirements  

Lab:

  • Stand for extended periods of time with periodic stooping / bending / kneeling
  • Able to lift, push, pull up to 50lbs.
  • Climb ladders and stairs of various heights.
  • Work in a lab environment requiring special protective clothing over the head, face, hands, feet, and body. This role requires the ability to wear personal protective equipment.
  • Certain tasks may require use of a respirator; medical clearance will be required in advance.

Compensation Details:

  • Orbis Clinical is an equal opportunity employer that provides a reasonable range of compensation for our positions. Actual compensation is influenced by a wide array of factors including, but not limited to, skill set, level of experience and specific office location.
  • The Pay Range for this position is $51.72 per hour, can vary depending on employment status.
  • Orbis Clinical offers eligible employees health benefits (medical, dental, and vision), employer-paid basic life and AD&D insurance, and a partial employer match on a 401(k). 

 

EEO and Reasonable Accommodation Statement:

Epic Staffing Group 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, genetic information, veteran status, or any other characteristic protected by law. We also consider qualified applicants with criminal histories, consistent with applicable law. If you need assistance or an accommodation during the application process, please contact us.

 By applying for this position, you agree that any calls from Orbis Clinical and its subsidiaries may be monitored or recorded for training and quality assurance purposes.


The Company is an equal opportunity employer and makes employment decisions on the basis of merit. The Company prohibits unlawful discrimination on the basis of race, color, national origin, ancestry, religion, creed, age, sex, sexual orientation, gender identity, pregnancy, marital status, physical or mental disability, medical condition or any other consideration made unlawful by federal, state or local laws. The Company will also provide reasonable accommodation to the known physical or mental disability of an otherwise qualified employee or applicant. Should you need any such accommodation, please contact the Company for further information. The Company is dedicated to ensuring that all decisions regarding personnel are in accordance with all applicable laws. I certify that all statements made in this application are true to the best of my knowledge. I understand that all falsification or misleading information given in my application may result in the termination of my employment with Orbis Clinical and its subsidiaries. Furthermore, I understand that my professional conduct and clinical performance is directly related to my ability to be placed on assignments for Orbis Clinical and that I will adhere to all regulations and guidelines of Orbis Clinical. I authorization Orbis Clinical to verify the information I have provided, to contact references, and to conduct criminal, education and personal background checks concerning my qualifications, and past employment record. I understand that nothing contained in this application is intended to create an employment contract, either verbal or written, with Orbis Clinical or its clients. Furthermore, I understand that my employment, it is “at will” and Orbis Clinical or I may terminate my employment at any time with or without notice and with or without case. I acknowledge that I will be legally obligated by the terms of this document by typing my name, which will constitute my signature, or manually signing, in the provided space and electronically transmitting this document to Orbis Clinical. I agree that Orbis Clinical and I may use electronic means to conduct this transaction and that this document shall be governed and construed by the laws of the State of Massachusetts.