Group Leader, Analytical Research & Development at CATALENT CTS SINGAPORE PRIVATE LIMITED

St. Petersburg, Florida, United States -

Full Time

Start Date

Immediate

Expiry Date

05 Jun, 26

Salary

0.0

Posted On

07 Mar, 26

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Analytical Research & Development, Project Management, Teamwork, Cross-functional Collaboration, Laboratory Supervision, Root Cause Analysis, Process Improvement, Customer Interaction, Training, Performance Evaluation, Development Plans, Supplier Qualification, Softgel Platform, GMP Compliance, Quality Control

Industry

Pharmaceutical Manufacturing

Description

Group Leader, Analytical Research & Development Position Summary Work Schedule: Standard Hours; Monday through Friday 100% on-site Join Catalent’s flagship softgel development and manufacturing facility in North America, located in St. Petersburg, FL, with a capacity of 18 billion capsules per year. This role offers competitive pay, day-one benefits, and career growth in a state-of-the-art, turn-key facility. As a Group Leader in Catalent’s Analytical Research & Development group, you’ll gain unmatched exposure to a diverse range of molecules formulated within the softgel platform, each with a unique purpose and direct impact on patients. Our work spans a wide range of therapeutics, from women’s health and prescription medicines to oncology, offering an experience few organizations can match. Through strong teamwork and cross-functional collaboration from development through commercial validation, you’ll build a rewarding career while helping deliver life-changing treatments to patients. The Role Prepare and set the daily work schedule for the Analysts by working with the Project Management and Customers to determine business needs. Directs and motivates the Analysts to meet or exceed the needs of the organization. Guides the Analysts by setting Laboratory targets and by providing clear instruction and guidelines for performance. Supervises Laboratory personnel for the following activities: Analysis of finished products, in-process materials, fill moisture, raw materials, and cleaning verification and Validation samples according to the assigned specifications, methods, and protocols. Preparation of reagents/standards/medias needed for analysis according to established methods. Records actual performance against the time schedule. Monitors progress of work against expectations. Identifies and implements process improvements that will reduce cycle time to test and release products. Conducts and writes laboratory investigations using the appropriate Root Cause Analysis tools. Identifies deviations if any and taking appropriate actions. Reports anomalies to management. Interacts directly with customers, both internal and external. Maintains discipline within the organization through effective motivation which includes effective training, clear instructions, clear performance standards, consistent and timely assessment/evaluation against the standards, consistent and timely feedback, appropriate disciplinary actions, including preparation and implementation of development plans as appropriate. Provides project support for new product development and Supplier Qualification requiring a close working relationship directly with Customers as well as suppliers. Perform other duties as required. Qualifications Bachelor’s degree in a scientific field with 10 years in lab; 9 in GMP or Master’s degree in a scientific field with 8 years in lab; 6 in GMP or Doctorate in a scientific field with 5 years in lab; 3 in GMP Minimum of 4 years in people management Individual may be required to sit, stand, walk regularly and occasionally lift to 15 pounds; no lifting greater than 44.09 pounds without assistance. Be accessible to manufacturing floor and office staff and to use required office equipment. Vision requirements include ability to differentiate color (Pass the Ishihara Color Vision Screening) and obtain 20/30 acuity in both far and near vision with or without corrective lenses. For Catalent’s in-house screening, the acceptable score is to identify at least 4 of 6 numbers in the circles. Why You Should Join Catalent Tuition reimbursement to support educational goals WellHub program to promote physical wellness & Access to Perkspot discounts from over 900 merchants 152 hours of PTO plus 8 paid holidays Medical, dental, and vision benefits effective day one Defined career path with annual performance reviews & strong potential for career growth within a mission-driven organization Inclusive culture with active Employee Resource Groups & Community engagement and green initiatives Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE. Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.

How To Apply:

Incase you would like to apply to this job directly from the source, please click here

Responsibilities

The Group Leader will prepare daily work schedules for Analysts, direct and motivate staff to meet organizational needs, and supervise laboratory personnel conducting various analyses on finished products, raw materials, and validation samples. This role also involves conducting laboratory investigations, identifying deviations, implementing process improvements, and interacting directly with internal and external customers.