The U.S. Pharmacopeial Convention (USP) USP is an independent scientific organization that collaborates with the world’s top experts in health and science to develop quality standards for medicines, dietary supplements, and food ingredients. Product Management Specialist vacancy is published now and interested candidates can apply online for Latest BSc Chemistry Job.
Position – Product Management Specialist
Location – Serilingampally Mandal, Ranga Reddy District, India
Brief Job Overview-
The Product Management Specialist main responsibilities will be supporting the USP Pharmaceutical Analytical Impurities (PAI) product pipeline through identification and evaluation of relevant materials. In addition, the individual will be responsible for building knowledge and expertise in adjacent areas including Active Pharmaceutical Ingredients (APIs), dissolution media, physiochemistry reagents, nano materials, extractables and leachables, and more to support the introduction of new products. The individual will work collaboratively within scientific and commercial teams.
The individual will be responsible for applying prioritization criteria, working closely with product management lead and others in the organization, to generate and evaluate target product lists utilizing process chemistry knowledge, collection, and review of pharmacopeial information, market information, peer reviewed publications, and patents, to determine and segment potential impurities by main manufacturing pathways. Responsibilities will also include support on intellectualproperty assessments to determine the freedom to operate.
The individual, working closely with Product Management leads, will maintain the list of target products, prioritization, and initiation of product development. The individual will work in a highly matrixed environment engaging with individuals across the organization including internal and external subject matter experts, marketing insights, strategic customer development, business development, and strategy to gain insight in market segments, and target customers, and develop commercial expertise in the life science space.
How will YOU create impact here at USP?
The position’s purpose should provide a high-level overview of why the position exists and briefly identify the most critical priorities of the position. This is an opportunity to highlight any features or duties of the role related explicitly to the Diversity, Equity, Inclusion & Belonging work of the Department.
- The primary objective is to collect data related to API manufacturing routes, identify the associated impurities, and identify the most critical ones. This will include utilizing process chemistry knowledge, collection, and review of pharmacopeial information, market information, peer reviewed publications, and patents, to determine and segment potential impurities by main manufacturing pathways.
- Additional objectives are to develop broad expertise in other areas to support new product introductions that will include API reference materials, dissolution media and reagents, physiochemistry reagents, nano materials, extractables and leachables and more for potential inclusion into the materials portfolio.
- Manage chemical information data through GSRS (Global Substance Registration System), excel and other systems.
- Develop commercial experience working closely with Product Management and commercial team in prioritizing items for inclusion in the portfolio and maximize product launches.
- Review of patents to determine the freedom to operate.
- Support comprehensive project management plans for various material segments.
- Participate in executing the change management plan.
The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience:
- Bachelor’s degree in Chemistry or a related field or equivalent relevant experience.
or a related field, or equivalent relevant experience.
- Three (3) to five (5) years of hands-on experience as a process chemist with exposure to many APIs and diverse types of APIs and knowledge of chemical supply/value chains.
- Experience with handling large amounts of data and information and using scientific databases
- Experience reviewing pharmaceutical patents and patent claims.
- Experience working on projects/products in life science industry, CRO/CDMO or equivalent relevant experience.
- Excellent organizational skills and use of excel and Microsoft Office suite.
Additional Desired Preferences for Latest BSc Chemistry Job
- Desired preferences are to showcase any additional preferred levels of expertise to perform the role. Reminder: any items listed in this section are not requirements nor disqualifies for candidate consideration.
- Knowledge of business practices and the pharmaceutical industry who is adaptive, industrious, analytical, and solution-oriented
- Workload management skills; able to juggle a diverse and rapidly changing workload, delivering across several teams within a matrixed structure
- Strong communication skills
- Experience collaborating effectively with other functional groups to achieve business objectives
- Results oriented with proven ability to work with a diverse range of collaborators
We are providing you with some of the expected interview questions and answers for the Latest BSc Chemistry Job. Kindly go through them and prepare well before you are going for the interview of Latest BSc Chemistry Job. All the best!!!
Question 1: Can you elaborate on your experience with identifying and evaluating impurities in the pharmaceutical industry, and how you’ve contributed to new product introductions?
“Throughout my career, I’ve worked extensively in the pharmaceutical industry, focusing on process chemistry and impurity analysis. In my previous role at XYZ Pharmaceuticals, I was responsible for identifying and characterizing impurities associated with various API manufacturing routes. This involved utilizing a combination of process chemistry knowledge, reviewing pharmacopeial information, and analyzing patents to segment potential impurities. Additionally, I collaborated closely with cross-functional teams to introduce new products, aligning my analytical insights with product development strategies. This experience has provided me with a solid foundation to contribute effectively to the identification and evaluation of materials in the pharmaceutical analytical space.”
Question 2: Could you discuss how you’ve managed and organized large amounts of chemical data and information to support decision-making in your previous roles?
“Managing extensive chemical data has been a crucial aspect of my roles. At my previous organization, I successfully implemented a structured data management process using tools like GSRS and Excel. This allowed me to efficiently organize, categorize, and retrieve chemical information, which was essential for identifying impurities and assessing potential product introductions. This approach enabled quicker decision-making and streamlined collaboration with cross-functional teams, ensuring that accurate data was readily available for evaluations.”
Question 3: How have you demonstrated your ability to work in a matrixed environment and collaborate effectively with internal and external stakeholders to achieve business objectives?
“I’ve thrived in matrixed environments, and my experience highlights this. In my previous role, I collaborated with subject matter experts, marketing teams, business development, and external partners to gather insights for impurity identification and product introductions. For instance, when introducing new products, I closely collaborated with product management and commercial teams to align priorities and strategies. This required effective communication, active listening, and adaptability to ensure that our initiatives were aligned with business goals and market demands.”
Question 4: Can you share an example of a project where you conducted a freedom-to-operate assessment based on patent reviews, and how it influenced decision-making?
“In a recent project at ABC Pharma, we were exploring the introduction of a novel API. I conducted a thorough review of relevant patents and analyzed patent claims to determine the freedom to operate within the competitive landscape. This assessment provided insights into potential legal hurdles and helped us make informed decisions regarding our product’s design and positioning. By proactively addressing potential patent conflicts, we not only ensured legal compliance but also enhanced our ability to enter the market with a competitive advantage.”
Question 5: How do you balance and manage your workload effectively when dealing with multiple teams and projects within a rapidly changing environment?
“Effective workload management has been a core aspect of my career. In my previous roles, I’ve been responsible for diverse projects that required juggling tasks across different teams. I prioritize tasks based on strategic importance and deadlines, ensuring that I allocate time for both short-term goals and long-term projects. I leverage tools like project management software to track progress and maintain clear communication with stakeholders. This approach has allowed me to adapt to changing priorities efficiently while consistently delivering high-quality results.”