Sr. Scientist, Formulations at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Collegeville, Pennsylvania, United States -

Full Time

Start Date

Immediate

Expiry Date

30 May, 26

Salary

0.0

Posted On

01 Mar, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Pre-formulation, Formulation Development, Process Development, Sterile Product Dosage Forms, Batch Manufacturing, Stability Studies, Clinical Trials Coordination, Data Recording, GMP, GLP, Technical Reporting, Problem Solving, Equipment Operation

Industry

Biotechnology Research

Description

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Role: Sr. Scientist This is a fully onsite role based at our customer’s site in Collegeville, PA. We welcome applicants from all locations within the US. Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate. Must be legally authorized to work in the United States without sponsorship. Must be able to pass a comprehensive background check, which includes a drug screening. Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission – to enable our customers to make the world healthier, safer, and cleaner. Within our Analytical Services team, we have a functional service provider solution, which is a unique partnership that allows our customers to demonstrate the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits. As a Scientist supporting the Pharm Dev Steriles in our client's Pharmaceutical R&D, you will have the opportunity to apply technical skills and expertise to develop drug product formulations and associated manufacturing processes as part of a matrix technical team. You will also use creative thinking to drive drug development of a variety of sterile product dosage forms Key Responsibilities: Completes pre-formulation, formulation and process development activities based on established protocols and procedures Assists in the manufacture of batches of product as required, e.g. for process development, stability studies or clinical trials Coordinates activities within Pharmaceutical Development and with analytical and manufacturing representatives to meet project results Works with the team to align and implement pre-formulation, formulation and process development activities including authoring or contributing to manufacturing batch records Identify and begin to interpret any problems in the execution of experimental processes and/or in results and communicates them to supervisor Proactively engage and seek assistance from other scientists to solve problems Maintains cleanliness in own work area and in communal work areas Anticipates/recognizes potential problems with equipment and/or supplies, and proposes/initiates action to solve or prevent problems Operates equipment for which is trained independently with due regard for GMP and Safety Demonstrates timely & reliable recording of laboratory data in Labware and other suitable systems in accordance with company policy and legal requirements. Performs data management tasks including recording results successfully and in compliance with departmental guidelines in a laboratory notebook or computer (e.g. tabulating and graphing results) Consults with supervisor when difficulties arise that cannot be readily resolved Prepares oral or written summaries of results with interpretation for project work Writes specific technical sections of internal and external reports with supervision Attends regular safety training and is fully aware of safety requirements for their laboratory/working environment Maintains accurate and complete safety records consistent with company policy and legal requirements Recognizes potential safety problems and takes action to resolve them Basic Requirements: BS degree with 4-6 years of experience in an appropriate subject area or a MS 2-4 years of experience in the subject area Is technically proficient in a number of formulation/process development techniques. Has good knowledge of GMP and GLP requirements, SOPs and policies Has operational knowledge of routine laboratory/plant equipment In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Benefits: We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation! Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued Thank you for your interest as you consider starting a new career journey with us. As the world leader in serving science, our colleagues develop critical solutions through innovation—and build rewarding careers. Discover their extraordinary stories and connection to our Mission to enable our customers to make the world healthier, cleaner and safer. Their work is a story of purpose. What story will you tell? Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of more than $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Thermo Fisher Scientific is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, creed, religion, color, national or ethnic origin, citizenship, sex, sexual orientation, gender identity and expression, genetic information, veteran status, age or disability status.

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Responsibilities

The Senior Scientist will apply technical expertise to develop drug product formulations and associated manufacturing processes for sterile dosage forms as part of a matrix team. Key duties include completing pre-formulation, formulation, and process development activities, assisting in batch manufacturing, and coordinating activities with analytical and manufacturing representatives.