What are the responsibilities and job description for the Scientist position at Veranova L P?
Company Description
Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation.
Job Description
Entry level PhD position for process research and development. A process research and development chemist is responsible for enabling the manufacturing of Active Pharmaceutical Ingredients (APIs) under cGMPs on larger scales in a safe and reliable manner through creating an understanding of how chemical processes work and how those chemical processes will translate from a laboratory to a manufacturing environment. The Scientist position requires the application of in-depth chemistry knowledge and standard laboratory techniques and procedures as well as an ability to make keen observations to solve more complex technical issues while learning about how other factors such as cGMPs and manufacturing equipment influence processes and decision making.
Key Responsibilities
Entry level PhD position for process research and development. A process research and development chemist is responsible for enabling the manufacturing of Active Pharmaceutical Ingredients (APIs) under cGMPs on larger scales in a safe and reliable manner through creating an understanding of how chemical processes work and how those chemical processes will translate from a laboratory to a manufacturing environment. The Scientist position requires the application of in-depth chemistry knowledge and standard laboratory techniques and procedures as well as an ability to make keen observations to solve more complex technical issues while learning about how other factors such as cGMPs and manufacturing equipment influence processes and decision making.
QUALITY/REGULATORY RESPONSIBILITIES
- Becomes technically proficient and self-assured in applying cGMP standards.
- Applies cGMP concepts in association with department specific responsibilities.
- Ensures all documentation produced is in compliance with governing SOPs.
- Responsible for contributing to audit readiness and for participating in quality audits with FDA, other Regulatory Agencies, and customers, as needed.
- Ensures work is in compliance with all state and federal regulations, including but not limited to GMP, DEA, FDA, etc.
ENVIRONMENTAL, HEALTH, & SAFETY RESPONSIBILITIES
- Follows and abides by all EH&S policies, practices, and procedures in association with department specific responsibilities.
- Demonstrates technical and procedural proficiency and self-assuredness in applying EH&S standards.
- Responsible for contributing to audit readiness and for participating in EH&S audits with internal Company groups, regulatory agencies, and customers.
- Responsible for reporting all near misses, accidents, and dangerous occurrences through the appropriate Company procedures to ensure an investigation is initiated.
- Cooperate with all root cause investigations and follow corrective actions and compliance with Company policies and procedures, and all state and federal regulations occurs within department.
- Support the Company’s commitment for environmental health & safety by applying ISO 14001, OHSAS 18001, and Sustainability 2025 principals into daily activities.
PHYSICAL DEMANDS & WORK ENVIRONMENT
- While performing the duties of this job it is required to stand, walk, and use hands to operate objects, tools, or controls; reach with hands or arms; climb, balance, stoop, kneel, or crouch when necessary for job activity.
- Must be able to lift and/or move up to 50 pounds.
- Specific vision abilities include: near, distance, peripheral, color perception, and the ability to adjust focus.
- Regularly works with moving mechanical parts and may work with toxic or caustic chemicals. The work may be performed in humid areas with low or high temperatures.
Qualifications
ESSENTIAL
- PhD in Organic Chemistry or equivalent with a minimum of 0-2 years of process development related experience in a pharmaceutical industry.
- MS in Chemistry or equivalent with a minimum of 8 years of process development related experience in a pharmaceutical industry.
- BS in Chemistry or equivalent with a minimum of 12 years of process development related experience in a pharmaceutical industry.
- Experienced in designing, developing, and optimizing synthetic routes, producing and/or scaling up intermediates and APIs.
- Experience with common analytical techniques such as: HPLC, GC, NMR, UV, LC-MS.
- Ability to read, analyze, and interpret English-language chemical periodicals, scientific journals, and regulatory documents.
- Ability to write clear and concise technical reports.
- Good understanding of Microsoft Office and other job-related software.
- Ability to define problems, collect data, recognize patterns, and draw conclusions from disparate information streams.
- Ability to plan, organize, and oversee independent research projects.
- Demonstrate ability to exercise good judgment and make decisions quickly.
- Good written and verbal communication skills.
- Experience communicating effectively to management.
- Ability to work independently and in a team environment.
- Good organization and prioritizing skills.
VALUED
- Knowledge of MS Project. Experience in establishing integrated plans with resource and task constraints.
- Experience with Design of Experiments (DoE)
- Hands on skills in Azure services (e.g. Data Factory, Data Lake, Functions, Logic Apps, Service Bus
- Azure DevOps (ADO) proficiency.
- Self-starter, able to work independently.
- Excellent communication (verbal and written) skills.
Additional Information
All your information will be kept confidential according to EEO guidelines.
Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age, race, color, national origin, religion, sex, sexual orientation, gender identity and/or expression, physical or mental disability, genetic information, citizenship, marital status, veteran status, or any other characteristic protected by federal, state, or local law.
All applications are carefully considered, and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice.