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12 Vantive Jobs

Research Associate II

8-14 years

Bangalore / Bengaluru

1 vacancy

Research Associate II

Vantive

posted 16hr ago

Job Description

  • Conducting laboratory testing, not limited to validation, verification, transfer, and registration stability studies.
  • The successful candidate shall possess solid hands-on technical abilities, a passion for their work and the impact it has on meeting the needs of patients.
  • Effectively contributing technical knowledge and skills to a variety of projects by conducting testing, and designing analytical methods and experiments.
  • Interacting effectively with a variety of disciplines (Quality, Regulatory, External partners, etc).
  • Conducting routine research and design experiments, independently developing / evaluating / validating and/or transferring analytical methods.
Essential Duties and Responsibilities:
  • Collect information for the analytical target profile.
  • Propose techniques and develop analytical methods independently.
  • Design studies and write protocols, reports, and procedures with minimal guidance.
  • Evaluation, validation, or transfer of analytical methods, including investigating failed acceptance criteria.
  • Contribute routine scientific knowledge or expertise to research and development activities for achievement of project goals.
  • Evaluation of current methods and devise new approaches through adaptations and incorporation of new technologies to meet business objectives such as quality and cycle-time.
  • Independently conduct routine research and developmental activities. Plan details of assigned tasks within specific parameters.
  • Employ appropriate techniques and methods to successfully conduct assignments within negotiated deadlines after receiving general instruction.
  • Perform laboratory testing in a regulated environment.
  • Demonstrate a working knowledge of basic technical theories and principles within the area of expertise for routine tasks.
  • Develop knowledge and understanding of GxP and related regulations and guidance.
  • Conduct R&D stability testing as per the stability protocol to support the registration of R&D Products.
  • Independently execute analytical method validations and transfers with minimal support.
  • Accurately test the samples (Right First Time) and assess results for conformance to specifications.
  • Manage Laboratory investigations (OOS/OOT) and nonconformance/deviations to identify sound scientific root causes to follow the implemented corrective and Preventive actions.
  • Sample receiving and data entry in LIMS.
  • Adhere to cGxP requirements (ALCOA+), Data Integrity, Quality Culture and Compliance Level.
  • Own SOPs of relevant techniques/procedures.
  • Advise and troubleshoot issues and propose solutions.
  • Maintain lab equipment and report on malfunctions.
  • Good knowledge of laboratory health and safety standards.
  • Demonstrate the ability to identify risks, and issues, and identify opportunities for improvement of existing processes, technologies, and approaches by providing a sound scientific rationale.
  • Maintain knowledge of relevant QSR and other regulatory requirements related to R&D to ensure compliance in all research, data collection, and reporting activities.
  • Collaborate with global teams across various functions (ex. quality, regulatory, operations, manufacturing, etc).
  • Analyze data, make decisions, and present status at technical review meetings.
  • Design studies and autonomously write protocols, reports, and procedures with minimum guidance.
  • Support in writing responses to authorities questions on analytical methods.
Qualifications:
  • Strong knowledge of regulatory validation & stability guidelines and skills for testing products within relevant disciplines.
  • Possess relevant good practical knowledge of analytical techniques like HPLC/UPLC, GC, Titrations, AAS, etc,
  • Possess relevant laboratory/technical, writing, and computer skills.
  • Able to work in a team environment appropriately supporting others.
  • Self-motivated and takes personal responsibility for getting the job done.
  • Ability to objectively assess, organize, and communicate complex information.
  • Understand the importance of project schedules and contribute to efforts beyond their scope of responsibilities to ensure project milestones are met.
  • Ability to adapt to shifting priorities.
  • Ability to demonstrate critical thinking and problem-solving skills.
  • Handling of software like Empower, Chromeleon, LIMS, etc,
  • Good learning agility and communication skills.
  • Possessing relevant computer and technical skills including M.S Word, spreadsheets etc
  • bachelors degree with 8-14 years or masters degree with 5 to 10 years of experience in a relevant scientific discipline (Analytical chemistry/Pharmaceutical chemistry)

Employment Type: Full Time, Permanent

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