Scientist - Microbiology, HPLC

Scientist - Microbiology, HPLC

04 May 2024
Pennsylvania, Collegeville, 19426 Collegeville USA

Scientist - Microbiology, HPLC

Job DescriptionAt Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.Location/Division Specific InformationThermo 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 clients to make the world healthier, safer, and cleaner.Within our Analytical Services team, we have a functional service provider solution, which is an outstanding partnership that allows our customers to use 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.This is an onsite position located in Collegeville, PA.Discover Impactful WorkThe Scientist possesses a thorough understanding of laboratory procedures and can reliably conduct complex analysis with increased independence. Performs a variety of complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices. Follows validated or experimental analytical procedures with periodic direct supervision. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. Enters data into databases and reports. Performs self review for own data prior to QC submission.pA day in the Life:A day in the Life

Performs a variety of complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and /or biological matrices for stability and analytical testing.

Works with multiple functional groups to meet business needs.

Plans and organizes work with periodic supervision.

Sets up and maintains analytical instrumentation.

Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory procedures and guidelines.

Ensures QA findings are addressed appropriately.

Provides assistance and training to other team members.

Problem solving, either independently or with assistance pertaining to extraction and/or instrumentation problems.

Communicates project status to project leader.

Performs work assignments accurately, and in a timely and safe manner.

Reviews, interprets, and analyzes data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP). Performs self and peer review of the data for accuracy and compliance with reporting requirements prior to submission to QA and issuance to customers.

Keys to SuccessEducation and Experience

Bachelor's degree or equivalent and relevant formal academic / vocational qualification

AND 2+ years of previous experience that provides the knowledge, skills, and abilities to perform the job.

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.Knowledge, Skills, Abilities

Demonstrated knowledge of multiple applicable techniques such as: HPLC, GC, MS, Dissolution

Testing, Inhalation Testing, Biopharmaceutical Testing, Karl Fischer, UV-Vis, FT-IR, TOC

Proficient in Microsoft Excel and Word

Proven ability to interpret data by performing trend analysis

Proven ability in technical writing skills

Ability to independently optimize analytical methods

Proven problem solving and troubleshooting abilities

Good written and oral communication skills

Time management and project management skills

Ability to work in a collaborative work environment with a team

Physical Requirements / Work EnvironmentThermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:

Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.

Able to work upright and stationary and/or standing for typical working hours.

Able to lift and move objects up to 25 pounds.

Able to work in non-traditional work environments.

Able to use and learn standard office equipment and technology with proficiency.

May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.

Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.

BenefitsWe 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.Apply today! http://jobs.thermofisher.comThermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.Accessibility/Disability AccessJob Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1-855-471-2255. Please include your contact information and specific details about your required accommodation to support you during the job application process.This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Related jobs

  • Medical Information (MI) is a global customer-focused group that provides a scientific service for responding to unsolicited medical inquiries regarding Pfizer products. Key expectations for this role include executing core MI science-related activities for a designated portfolio by leveraging expertise with MI science skills in ensuring the delivery of high quality medical and scientific information to health professionals, patients, and external organizations, as well as contributing to MI initiatives with Business Unit(s), Product/Therapy Area Team(s), and other platform functions in support of departmental and company objectives. The scope of responsibilities will include Local, Regional (above country) and Global elements. Additionally, a Manager, Medical Information Scientist is expected to actively contribute to relatively complex projects/initiatives.

  • Reference #: 394950 Site Name: USA - Pennsylvania - Upper Providence Posted Date: Apr 26 2024

  • Job Description

  • Reference #: 259309 This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following Plan, design and execute work/experimental programmes to further the course of Discovery and Development Projects / programmes and enable key decisions, in particular using mass spectrometry (both LC-MS and GC-MS qualitative). Demonstrate a sound practical understanding of mass spectrometry and processes, procedures used in mass spectrometry. Contribute to regulatory dossiers and author/review expert reports. Comply with the requirements of Quality, Safety and GSK policies and procedures and ensure that GSK intellectual property is protected. Ability to contribute to and effectively work within matrix teams and with colleagues in other divisions and also colleagues in same divisions e.g. NMR. Self-motivated flexible approach with good organisational skills and ability to communicate in a scientific manner. Working knowledge of GxP requirements, SOPs and policies. Appropriate knowledge of regulatory requirements as applied to the drug development process. Operational knowledge of laboratory/plant equipment. Why you?

Job Details

Jocancy Online Job Portal by jobSearchi.