Biochemist job description

Quidel's mission is to provide patients with immediate and frequent access to highly accurate, affordable testing for the good of our families, our communities and the world. We are a leading manufacturer of point of care diagnostic solutions. Quidel's comprehensive product portfolio includes tests for a wide range of infectious diseases, cardiac and autoimmune biomarkers, as well as a host of products to detect COVID-19.

We are excited to announce that Quidel Corporation is now becoming QuidelOrtho! This transaction will bring together two world-class teams and complementary product portfolios to serve patients around the world. During this transition period, we encourage you to continue visiting our career site and also check out more career opportunities at Careers at Ortho Clinical Diagnostics | Ortho Clinical Diagnostics jobs Join our journey as we become one global diagnostics leader!

The Molecular Biochemist is responsible for small to mid-scale purification of proteins and relevant quality control activities, as well as supporting research and new product development. Responsibilities may include maintenance for GMP protein production and providing support in addressing issues that may cause product supply interruptions.

ESSENTIAL FUNCTIONS:Follow GMP manufacturing and QC protocols.Independently plan and execute experiments.Resolve product performance issues.Summarize experimental data, draws conclusions and makes recommendations to manager.Maintain detailed and organized GMP documentation and laboratory notebooks in accordance with both internal and external regulatory requirements as part of the protein production process.Maintain a safe working environment.Develop raw material, in process, and product specifications.Support development of QC standards and test methods.Participate in team environment and interacts with team members professionally.Attend product development as needed.

EDUCATION AND EXPERIENCE:BA/BS in life sciences and/or skills usually associated with 2-4 years of relevant industrial experience or MA/MS in life sciences plus 1-2 years' experience.

KNOWLEDGE/SKILLS:Background in chemistry, biochemistry, molecular biology, virology, immunology, or related field required.Knowledge of scientific principals and concepts.Hands on expertise performing protein purification (column based methods, gravity flow). Experience with AKTA instrument preferred. Experience with general molecular biology skills such as PCR amplification, primer design, gel electrophoresis and bacterial transformation preferred.Protein optimization laboratory research experience preferred, particularly in recombinant protein expression.Good organizational skills and an ability to perform multiple tasks simultaneously required.Good ability to prepare and present technique data required.Strong analytical and problem solving skills.Ability to work within cross-functional teams.Demonstrate ability to consistently meet proposed objective timelines.Excellent communication skills (verbal and written) required.Must exhibit professionalism and maturity and display desire to succeed, be self-motivated and proactive required.Working knowledge of GMP and ISO 13485 quality system regulations preferred.Appropriate computer skills (e-mail, graphing software, word processing) required.Must possess ability to develop experimental plans and execute associated activities per communicated timelines.
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Before you apply, please make sure you share Quidel' s values. We pride ourselves on keeping these values in mind every day as we execute on goals and plan for the future. We are seeking employees who share the same mindset and commitment to be customer driven, focused on execution, and new product oriented. We succeed by being determined, optimistic team players.

Quidel is proud to be an Affirmative Action/Equal Opportunity Employer (Minorities/Women/Disabled/Veterans). We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Job Title
Biochemist - GMP
Location(s)
San Diego - BioLegend
BioLegend, Inc. (a PerkinElmer Company) develops world-class, cutting-edge antibodies and reagents for biomedical research, manufactured in our state-of-the-art facility in San Diego, CA. Our mission is to accelerate research and discovery by providing the highest quality products at an outstanding value, along with superior customer service and technical support. Our product expertise covers a diverse set of research areas including Immunology, Neuroscience, Cancer, Stem cells, and Cell Biology.

In 2021, PerkinElmer, Inc. (NYSE: PKI) a global leader committed to innovating for a healthier world, acquired BioLegend. The acquisition, the largest in PerkinElmer's history, further expands the Company's life science franchise into high-growth areas such as cytometry, proteogenomics, multiplex assays, recombinant proteins, magnetic cell separation and bioprocessing.

Job Summary
This position is responsible for different stages of manufacturing of various BioLegend's regulated product produced in our US FDA registered cGMP manufacturing facility.

The candidate will be responsible for formulating, filling, capping, labeling, completing batch records, putting away finished good inventory (FGI), data entry, equipment maintenance and supply inspections & storage.

Other responsibilities include purification of monoclonal antibodies derived from tissue culture material through an AKTA system. As well as the conjugation of purified antibody through the AKTA system. Buffer preparation and inspection of incoming buffers into the GMP suite will also be performed.

Another part of the job responsibility includes preparing product/project related documentation and maintaining the device history records for all the regulated products. Working closely with product development on new products in order to establish a smooth transition into manufacturing will also be required.

The desired candidate must be a team-player who is organized and has strong verbal and written communication skills and is able to work in a very fast paced environment. Great attention to detail is also a skill that will allow the candidate to be successful. The candidate must also be able to work independently and meet deadlines.

Essential Functions
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Prepare various buffers for manufacturing activities.Perform incoming inspection of raw materials.Perform formulation and vialing of the regulated products.Assist in troubleshooting the manufacturing process.Maintain batch records and other documentations that are essential to be in compliance with ISO13485:2016 and cGMP.Maintain/troubleshoot laboratory equipment and manage supplies.Process purification or conjugation orders as needed through the AKTA system.Perform dialysis, centrifugation, and column chromatography.Conduct Endotoxin tests.Advance multiple projects simultaneously and work in a team environment.Other projects or responsibilities as may be required.

iACT Competencies
innovate - Be better, keep improving, be more efficient, creative, and be in the forefront of development Aspire - Have desire, purpose, and ambition challenging ourselves to push the limits and reach new heights Collaborate - Foster teamwork, common goals, selflessness, communication and mutual support Transform - Adapt, learn, re-invent and change for future development and growth
Minimum Qualifications - Education and Experience
Bachelor's degree with some industry experience.

Preferred Qualifications - Education and Experience
Bachelor's degree with a minimum of 1-year Lab experience.

Work Environment & Physical Demands
Lab
While performing the duties of this job, the employee regularly works in a laboratory environment with occasional data entry on a computer. Occasional exposure to a warehouse environment.

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.

While performing the duties of this job, the employee is regularly required to use hands and fingers to handle, feel, or operate objects, tools or controls, and reach with hands and arms. The employee is frequently required to stand, talk and hear.
PerkinElmer is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability status, age, or veteran status or any other characteristics protected by applicable law. PerkinElmer is committed to a culturally diverse workforce.

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 are approx. 3 billion Euros turnover, 800 laboratories across 44 countries and more than 50.000 staff.
Employee Responsibilities:

* Performing stability and release testing in support of large molecule biopharmaceutical products using various analytical techniques including HPLC, SCE, CE, iCE, UV, MFI, Appearance, etc.

* Document work as required for cGMP compliance

* Perform tests accurately
* Troubleshoot method and instrumentation problems
* Use Office and instrumentation specific computer software including Empower

The Ideal Candidate would possess:

* Strong computer, scientific, and organizational skills

* Excellent communication (oral and written) and attention to detail

* Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude

* Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies

* Theoretical understanding of large molecule biochemistry

Minimum Qualifications:

* Bachelor's degree in biochemistry, biology, chemistry, biology, or other related degree concentration or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major)

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

Position is full-time, Monday-Friday, 7AM- 4 PM or 3 PM- 12:00 AM. Candidates currently living in a commutable distance to Lancaster, 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.