Summary
Overview
Work History
Education
Skills
Additional Information
Personal Information
Responsibilities
Timeline
Generic

Omotayo Odiwo

Summary

Accomplished and highly driven Associate Director of Laboratory Resources with experience overseeing laboratories and chemical research, collaborating with quality control teams, and implementing innovative solutions that ensure equitable pharmaceutical products. A transformational industry expert who accurately identifies required delivery and process improvements that drive increased efficiency, throughput, and quality. Meticulous Chemist and highly analytical thought leader with a proven track record managing large- and small-scale projects, developing pharmaceutical products, improving opportunities, organizing prioritization, and aligning resources. Highly organized and self-motivated professional experienced in project management, team development and process improvement. Skilled in developing and implementing strategies to increase efficiency and performance. Passionate about driving business growth and creating positive work environment. Hardworking Associate Director knowledgeable about business practices in the Pharmaceutical industry. Adept at supporting and enhancing operations with a decisive leadership style and strategic approach to decision making. Strong leader and problem-solver dedicated to streamlining operations to decrease costs and promote organizational efficiency. Uses independent decision-making skills and sound judgment to positively impact company success. Encouraging manager and analytical problem-solver with talents for team building, leading and motivating, as well as excellent customer relations aptitude and relationship-building skills. Proficient in using independent decision-making skills and sound judgment to positively impact company success. Dedicated to applying training, monitoring and morale-building abilities to enhance employee engagement and boost performance. Seasoned Assistant Director knowledgeable about all areas of business operations. Offering 21 years of experience in business planning, operations and team management. Strong leadership and team-building skills. Collaborative leader with dedication to partnering with coworkers to promote engaged, empowering work culture. Documented strengths in building and maintaining relationships with diverse range of stakeholders in dynamic, fast-paced settings. Organized and dependable candidate successful at managing multiple priorities with a positive attitude. Willingness to take on added responsibilities to meet team goals.

Overview

24
24
years of professional experience

Work History

Associate Director of Laboratory Resources

Lloyd Inc
09.2017 - Current
  • Led teams of up to 25 personnel, supervising daily performance as well as training and improvement plans.
  • Trained and developed department leaders and management staff for specific projects and ongoing operational needs.
  • Managed cross-functional teams for multiple large-scale projects, successfully completing each on time and within budget constraints.
  • Mentored junior staff members, providing guidance on professional development opportunities and career progression paths within the company.
  • Ensures equipment, facilities and maintained in clean, good operating condition.
  • Established strong relationships with key industry partners, creating mutually beneficial opportunities for growth and collaboration.
  • Improved overall team efficiency by streamlining project management processes and implementing new collaboration tools.
  • Oversaw annual budget planning processes, ensuring financial goals were met while maintaining optimal resource allocation across departments.
  • Reduced operational costs by identifying inefficiencies and implementing cost-saving measures in various departments.
  • Enhanced employee performance through targeted training programs and regular feedback sessions, resulting in higher productivity levels.
  • Promotes a customer focused right first time manufacturing environment.
  • Reviews and approves SOP, qualification and validation documentation and technical reports.
  • Negotiated favorable contract terms with vendors and suppliers, resulting in significant cost savings without sacrificing service or quality standards.
  • Maintained compliance with industry regulations while adapting to changes in legislation or best practices as needed. GMP, FDA,USP, EP, JP, GLP, ICH and OSHA.
  • Managed data transfers and proactively resolved issues at manufacturing sites through effective troubleshooting.
  • Establish and ensure that all laboratory activities and records(e.g, SOPs, Calibration and instrument logs,OOS investigations) are properly documented and checked.
  • Championed corporate social responsibility initiatives that enhanced company reputation while positively impacting local communities.
  • Review Master Batch Record when changes occur and new product are developed.
  • Contribute to drug submissions for the FDA.
  • Provide overall technical leadership to the manufacturing team while at the same time promoting operational excellence.
  • Fostered a culture of continuous improvement by encouraging staff to share innovative ideas and providing resources for professional development.
  • Prioritized tasks and allocated resources appropriately to keep teams focused and productive.
  • Assisted senior leadership in managing all aspects of operations.
  • Trained and mentored new employees on industry practices and business operations.
  • Created and updated physical records and digital files to maintain current, accurate, and compliant documentation.
  • Tracked key business metrics and made recommendations for proactive adjustments to policies and procedures.
  • Evaluated employee performance and conveyed constructive feedback to improve skills.
  • Recruited, interviewed and hired employees and implemented mentoring program to promote positive feedback and engagement.

Team Leader

PFIZER
01.2008 - 01.2017
  • Manage and oversee the Quality Control laboratories to include Production, Raw materials, Stability and Microbiology.
  • Supervised team members to confirm compliance with set procedures and quality requirements.
  • Monitored team performance and provided constructive feedback to increase productivity and maintain quality standards.
  • Built strong relationships with customers through positive attitude and attentive response.
  • Set performance expectations for the team, monitoring progress towards goals and providing constructive feedback as needed.
  • Empowered team members by delegating responsibilities according to individual strengths and areas of expertise.
  • Conducted training and mentored team members to promote productivity, accuracy, and commitment to friendly service.
  • Managed conflict resolution among team members, fostering a positive and collaborative work environment.
  • Developed team members'' skills through targeted coaching sessions, resulting in improved individual performance.
  • Mentored and guided employees to foster proper completion of assigned duties.
  • Held weekly team meetings to inform team members on company news and updates.
  • Provided ongoing support to direct reports, addressing concerns or questions promptly so they could remain focused on their tasks.
  • Monitored time and attendance, enforcing compliance with company procedures relating to absenteeism.
  • Assisted in recruitment of new team members, hiring highest qualified to build team of top performers.
  • Communicated KPIs outlined in annual plan to inform employees of expectations and deliverables.
  • Implemented employee recognition programs that boosted morale and increased retention rates within the team.
  • Evaluated staff performance and provided coaching to address inefficiencies.
  • Collected, arranged, and input information into database system(LIMS)
  • Orchestrated investigation on Laboratory OOS and OOT test result to ensure thorough root cause analysis and documentation.
  • Accurately assessed and approve technical protocol and reports to support validation and qualification activities.

Senior Laboratory Analyst

PFIZER
01.2000 - 01.2008
  • Led scheduling, product monitoring, utility monitoring, and testing performed by QC Laboratory.
  • Prepared samples and assisted laboratory personnel in performing qualitative and quantitative analysis using analytical instruments, techniques and methods(e.g, GC-MS, HPLC-MS, UPLC, ICP, IR, pH, SG, MELTING POINT.
  • Successfully initiate test method transfers by interpreting and recommending acceptable criteria.
  • Manage performance of QC sampling and testing primarily drug product, APIs, in-process and finished products.
  • Assisted in ordering laboratory supplies and necessities to maintain appropriate level of inventory.
  • Troubleshot instrumentation issues, reducing downtime and ensuring optimal performance of laboratory equipment.
  • Operated and troubleshot equipment, instruments and associated software and routinely performed quality control on instrumentation to comply with established specifications.
  • Enhanced data accuracy through diligent quality control measures and thorough documentation practices.
  • Participated in external audits, demonstrating compliance with regulatory requirements and industry best practices.
  • Actively contributed to the continuous improvement efforts within the lab by identifying opportunities for process enhancements or cost-saving measures.
  • Trained new hires on company policies, laboratory protocols, instrument operation, data analysis techniques, promoting a positive work culture.
  • Served as an effective liaison between the lab team and other departments, fostering successful cross-departmental collaboration.
  • Conducted routine maintenance on laboratory equipment to prolong lifespan while mitigating costly repairs or replacements.
  • Monitored and documented safety standards to verify compliance.




Additional Experience: Chemist at Aldrich Chemical company, Chemist at Chem-Met Services and Senior Chemist for Nigerian National Petroleum Corporation.

Education

Bachelor of Science in Chemistry -

Oglethorpe University
Atlanta, GA
05.1982

Skills

  • Pharmaceutical Portfolios
  • Chemistry
  • SOPs
  • Patient Advocacy
  • Laboratory Safety
  • Risk Management
  • Process Improvement
  • Manufacturing
  • Health Equity
  • CGMP
  • Biotech
  • Analytical Testing
  • Audits
  • Strategic Planning
  • Project Management
  • Strategic leadership
  • Coaching and Mentoring
  • Analytical Thinking
  • Hiring and Training

Additional Information

Mass Spectrometry, Dissolution Analysis, Strategic Planning, Technical expertise in HPLC, GC, UPLC(Agilent system) and Physical analysis(LOD, ROI, SG ETC), Quality Control, Laboratory Management, Interpersonal Communications, Corrective/Preventative Action, Experience in managing a 21CFR11 AND 21CFR111 cGMP compliant laboratory., USP, EP, JP and BP Pharmacopeias., Project Management, Experience with cGMP and FDA audits., Leadership & Team Building, OOS/OOT Investigation, Microbial limit Testing., Understanding of (CAPA) and (CLIA) Proficiency Programs., Project Management - Excels at planning, organizing, motivating, and controlling resources, procedures, and protocols in order to achieve specific goals., Leadership & Team Building - Committed to building cohesive teams and leading them down positive paths that increase knowledge and productivity.

Personal Information

Willing To Relocate: Anywhere

Responsibilities

  • Performance management and development of staff.
  • Partner within Quality control and across functional disciplines to influence and implement the technical agenda, site business plan objectives and GMP Plan objective.
  • Interact with regulators, customers,or other outside stakeholders on business issues or in support of internal and external agency audits.
  • Responsibilities include interviewing, hiring, and training employees, planning, assigning and directing work, appraising performance,rewarding and disciplining employees. addressing complaints and resolving problems.
  • Oversee all Release and stability analytical testing to ensure testing is timely and performed in compliance with cGMP, ensure product is released in a timely fashion.
  • Perform QC review of in-process and release data and certificate of Analysis per internal timelines, to support lot disposition.
  • Responsible for Quality System records associated with analytical testing(change control, lab investigations, OOS, deviations and CAPAs).
  • Assure ongoing readiness for regulatory inspection; participate in audits and inspection, and prepare responses to correspondence and findings as needed.

Timeline

Associate Director of Laboratory Resources

Lloyd Inc
09.2017 - Current

Team Leader

PFIZER
01.2008 - 01.2017

Senior Laboratory Analyst

PFIZER
01.2000 - 01.2008

Bachelor of Science in Chemistry -

Oglethorpe University
Omotayo Odiwo