In Process Analytical Scientist

Eurofins Scient. West Point , PA 19486

Posted 2 months ago

Eurofins Scientific is an international life sciences company which provides a unique range of analytical testing services to clients across multiple industries. The Group believes it is the world leader in food, environment and pharmaceutical products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and for supporting clinical studies. In addition, Eurofins is one of the key emerging players in specialty clinical diagnostic testing in Europe and the USA.

Group's key figures (as of March 2019) are approx. 3.8 billion Euros turnover, over 800 laboratories across 47 countries and about 45,000 staff.

In Process Analytical Scientist responsibilities include, but are not limited to, the following :

  • Must have skills in data analysis/interpretation, and the ability to exercise scientific judgment and for real-time decision-making.

  • Must be able to work both independently and within multi-functional teams in a fast-paced environment. Ability to work with little supervision and manage/differentiate ambiguous situations is important.

  • Must have communication and documentation skills, including result reporting skills (i.e. presentation of results, impact, and recommendations)

  • Must have demonstrated ability to work with others

  • Must continue to progress towards achieving qualification on the VFAE assay by completing training on required skills.

  • Titer testing is required for this position. Employment is contingent upon demonstration of a positive titer against the Varicella (chickenpox) virus.

  • The ability to work a flexible, rotating shift schedule, which will be predominantly nights and weekend coverage, will be required based on manufacturing process support needs.

The ideal candidate would possess:

  • Experience with flow cytometry (clinical flow cytometry is a plus) and/or performing immunoassays is preferred. Experience in analytical testing utilizing a variety of biochemical, molecular, and cell biology techniques.

  • Experience in laboratory operations including scheduling, equipment maintenance, and GMP documentation.

  • Experience with cell culture and aseptic techniques.

  • Good general industrial process knowledge and experience with cGMP manufacturing and/or large-scale production.

  • BS in life science (e.g., biology, microbiology, immunology, etc.), or engineering (e.g., biomedical, chemical).

  • Authorization to work in the United States indefinitely without restriction or sponsorship

Position is full-time, Monday-Friday, 8 a.m.-5 p.m., with overtime as needed. Candidates currently living in a commutable distance to West Point, PA are encouraged to apply.

What we Offer:

  • Excellent full time benefits including comprehensive medical coverage, dental, and vision options

  • Life and disability insurance

  • 401(k) with company match

  • Paid vacation and holidays

Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.


icon no score

See how you match
to the job

Find your dream job anywhere
with the LiveCareer app.
Mobile App Icon
Download the
LiveCareer app and find
your dream job anywhere
App Store Icon Google Play Icon
lc_ad

Boost your job search productivity with our
free Chrome Extension!

lc_apply_tool GET EXTENSION

Similar Jobs

Want to see jobs matched to your resume? Upload One Now! Remove
Associate Principle Scientist Vaccine Process Development And Commercialization (Downstream)

Merck & Co., Inc.

Posted 2 months ago

VIEW JOBS 3/5/2020 12:00:00 AM 2020-06-03T00:00 Job Description This role is for our Purification team in the Downstream area within the Vaccine Process Development and Commercialization (V-PDC) group which is in our Company's Manufacturing Division. V-PDC focuses on late stage process development, technology transfer, and in-line support of vaccine products. We seek an energetic, people-oriented leader with strong scientific, and technical skills to lead development, and commercialization activities supporting multiple vaccine programs. In this role, you will be responsible for: * Leading process development activities to execute large molecule upstream and/or downstream processing, including lab-scale process development, in-process assay support, and process scale-up/scale-down. * Execution of lab scale experiments, and authoring associated technical reports and documents. * Collaborating with commercial manufacturing teams to support facility start-up activities, and provide on-the-floor support for drug substance manufacturing, both within the our Company network and at contract manufacturing organizations (CMOs). * Leading assignment execution against accelerated, critical-path timelines in a right-first-time manner. * Authoring and/or reviewing technical documents to support Process Performance Qualification (PPQ) and licensure. * Provide mentor-ship and technical direction to other members of the team which may include dotted-line reporting relationships. Position Qualifications: Education Minimum Requirement: * Bachelor of Science (BS) in Chemical Engineering, Biochemical Engineering Bio-engineering, Pharmaceuticals, Biochemistry, Microbiology, or related field with ten years of relevant experience; or Masters degree with eight years of relevant experience; or Ph.D. with four years of relevant experience Required Experience and Skills * Large molecule process development or relevant experience, including scaling (up and down), and tech transfer of large molecule drug substance processes. * Hands-on expertise in execution of process development with multiple programs and unit operations across upstream and/or downstream unit operations. * Expertise in lab-scale experimental execution, and experience with Design of Experiments (DOE), statistical data analysis, and presentation of results/conclusions. * Experience authoring technical documentation to support regulatory submissions. * Outstanding communication and people skills. * Ability to foster a collaborative work environment focused on mentor-ship, coaching, and Subject Matter Expertise. * Subject Matter Expert development. * Experience with project strategic planning. Preferred Experience and Skills: * Knowledgeable in Drug Substance end-to-end process development. * Proficiency with downstream unit operations, including chromatography. * Strong cross-functional background, enabling teams to reach peak performance. * Ability to provide scientific mentor-ship and guidance to technical coworkers and colleagues within and outside our Company * Project management experience with the ability to lead teams * Experience with downstream unit operation mathematical modeling, theoretical scaling calculations, and computational fluid dynamics (CFD) modeling. * Experience with large molecule assay development and/or execution. * Experience with Quality by Design (QbD), Lean Six Sigma principles * Experience supporting/writing regulatory filings (IND, MAA, BLA) and inspections with multiple agencies (FDA, EMA, JNDA, TGA) . * Experience with on-the-floor Good Manufacturing Practice (GMP) manufacturing support including providing immediate responses on the shop floor to deviations and potential deviations. Our Manufacturing & Supply Division is committed to be the most trusted supplier of bio-pharmaceuticals worldwide. Our facilities, along with our external contractors, suppliers, and partners, create an interdependent global manufacturing network that's committed to delivering a high quality, reliable supply to customers and patients on time, every time. Who we are … Merck & Co., Inc., Kenilworth, New Jersey, USA is known as "Merck" in the United States, Canada & Puerto Rico. We are known as "MSD" in Europe, Middle East, Africa, Latin America & Asia Pacific. We are a global biopharmaceutical leader with a diverse portfolio of prescription medicines, oncology, vaccines and animal health products. We are driven by our purpose to develop and deliver innovative products that save and improve lives. With 69,000 employees operating in more than 140 countries, we offer state of the art laboratories, plants and offices that are designed to Inspire our employees as we learn, develop and grow in our careers. We are proud of our 125 years of service to humanity and continue to be one of the world's biggest investors in Research & Development. What we look for … In a world of rapid innovation, we seek brave Inventors who want to make an Impact in all aspects of our business, enabling breakthroughs that will affect generations to come. We encourage you to bring your disruptive thinking, collaborative spirit and diverse perspective to our organization. Together we will continue Inventing For Life, Impacting Lives while Inspiring Your Career Growth. INVENT. IMPACT. INSPIRE. NOTICE FOR INTERNAL APPLICANTS In accordance with Managers' Policy - Job Posting and Employee Placement, all employees subject to this policy are required to have a minimum of twelve (12) months of service in current position prior to applying for open positions. If you have been offered a separation benefits package but have not yet reached your separation date and are offered a position within the salary and geographical parameters as set forth in the Summary Plan Description (SPD) of your separation package, then you are no longer eligible for your separation benefits package. To discuss in more detail, please contact your HRBP or Talent Acquisition Advisor. MMDHJ VPDC If you need an accommodation for the application process please email us at staffingaadar@merck.com For more information about personal rights under Equal Employment Opportunity, visit: EEOC Poster EEOC GINA Supplement OFCCP EEO Supplement OFCCP Pay Transparency Rule We are an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations. Search Firm Representatives Please Read Carefully Merck & Co., Inc., Kenilworth, NJ, USA, also known as Merck Sharp & Dohme Corp., Kenilworth, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: Regular Relocation: Domestic VISA Sponsorship: Travel Requirements: 25% Flexible Work Arrangements: Shift: Valid Driving License: Hazardous Material(s): Number of Openings: 1 Merck & Co., Inc. West Point PA

In Process Analytical Scientist

Eurofins Scient.