Research Scientist III

Research Scientist III will serve as expert to support commercialization of solid dose nutritional and gummy products. They will be responsible for scale up of new products on any bulk or product issues during product lifecycle. They must meet with customers and lead technical discussions. They will be responsible for performing key development activities including authoring work instructions, performing extended testing on pivotal batches, and training and troubleshooting issues in manufacturing. They must be knowledgeable of dietary supplement ingredients and excipient function including physical and chemical properties. The candidate must be knowledgeable of cGMP and regulatory requirements and not debarred from activities related to food or drug manufacture (FDA). They must set an example by creating an open environment of mutual respect and honesty and by focusing on the facts and data. They must be comfortable with mentoring and supervising others.

Specific Responsibilities

• Leads and oversees full scale pivotal development batches completing all documentation in a timely manner with appropriate scientific rationale and justification where needed.
• Works closely with Quality and R&D colleagues to prepare, review master batch records, work instructions, specifications, position papers, CAPAs, MRBs and SOPs as needed. Write reports to capture all key data and rationale to validate manufacturing process for new products.
• Conducts scientific trials to support new raw sources and determine impact to product.
• Responsible as a technical task leader within his/her area of expertise on company project teams, communications with customer; Demonstrate the ability to resolve key technical hurdles and questions by effectively utilizing available information and technical expertise.
• Demonstrate the character of a science professional and a high degree of responsibility in maintaining scientific standards, cGMP compliance, and safe laboratory practices for self and reporting staff.
• Responsible for compliance with applicable corporate policies and procedures; Follows safety guidelines and policies when performing duties in the laboratory or manufacturing.
• Participates in dietary supplement related and science-based organizations, review industry updates, new guidance, new methods, etc. with these groups as the IVC representative.
• Maintains ethical and good character as an IVC employee always representing highest level of standards as cited in our employee handbook.

General Responsibilities

• Poses no direct threat to the health or safety of himself/herself, of others, or to property. Defined as a significant risk of substantial harm that cannot be eliminated or reduced to an acceptable level by reasonable accommodation.
• Requires regular attendance to perform essential element as contained herein between the assigned start and end times for work unless requested by management to fulfill a specific assigned duty to support manufacturing.
• Performs job tasks as needed to support manufacturing requiring technical expertise or insight.

The Candidate

Education, Experience, and Licenses:

Graduate degree (Masters or Doctorate) in food science formulation, chemistry, or pharmaceutics with at least 5 years of experience developing formulations and/or troubleshooting manufacturing supplement or drug products; Bachelors degree in Science in food science formulation, chemistry or pharmacy with at least 10 years experience developing formulations and/or troubleshooting manufacturing supplement or drug products; Licensed pharmacist with at least 5 years experience in industry with focus on formulation of oral products.

Knowledge, Skills, and Abilities

Excellent knowledge and experiences related to cGMP and regulatory requirements for NSF, USP and similar certifications.

Demonstrated good ability to resolve major technical challenges by effectively utilizing available information and technical expertise in manufacturing

Excellent time management, leadership, and communication skills (both oral and written).

Motivated leader for innovation and continuous improvements with colleagues, learns fast, grasps the "essence, and can change course quickly as required

Ability to build excellent relationships with quality and other colleagues; proactive and motivated for best-in-class timely task completions and team performances

International Vitamin Corporation (IVC) Is an Equal Opportunity Employer. Our organization remains steadfast in our commitment to fostering an inclusive and non-discriminatory work environment that welcomes individuals from all backgrounds. We firmly maintain the belief that every individual ought to be treated with respect and dignity, regardless of their race, color, religion, sex, sexual orientation, gender identity or expression, age, national origin, disability, veteran status, marital status, genetic information, or any other protected characteristic, as defined by the law. We pledge that all eligible job applicants shall receive an impartial and unbiased evaluation during the recruitment process, without any form of discrimination based on any of the protected class. Our dedication to promoting diversity and inclusivity remains unwavering, and we take immense pride in cultivating a workplace culture that values and celebrates differences. Our efforts towards creating an environment that is free from prejudice and discrimination are an integral part of our organizational philosophy, and we stand committed to upholding these principles.

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