Small Molecule Manufacturing Expert Jobs

Extensive knowledge and experience with brand management, media communication, advertising, sales, strategic and strategic marketing

Proven strategic brand planning, management, monitoring, and execution experience

Strong experience as a senior Marketing Leader in the Biopharma/Life Sciences space

Experience leading a team and creating/revamping a complete Marketing and brand strategy

Critical thinking skills and the ability to work in a fast-paced environment

Senior Director of Marketing - Responsibilities

Stock culture management and quality control of same

Microbiological media management and quality control of same

Research experiments as deemed appropriate by Merck management

Prepare GMP documentation as requested by management

Inform management of non-conforming events

Retrieve data when requested by Microbiology management

Experience working directly with Senior Management teams, as well as Partners and key decision makers in the space

Experience working in a senior business development position within a fast-paced and dynamic environment

Proven and successful experience in prospecting and lead generation

Entrepreneurial mindset with an outstanding knowledge of the market landscape

Chief Business Officer (CBO) - Responsibilities:

Chief Business Officer (CBO) - Requirements:

A comprehensive benefits package including a 401(k) with a company match.

You have payroll and sales tax knowledge as applicable to businesses.

Ensure an excellent customer experience using your expertise, resolving tax issues, and documenting your interactions.

Support, coaching, and continuous, real-time feedback.

You know the difference between LLCs, S-corporations, and C-corporations, and the tax issues relating to the election of these entity types.

You are friendly and reassuring, with a passion for customer service and problem resolution.

Report potential operational risks and issues to senior management and lateral operational managers

Conduct briefings and participate in technical meetings for senior management and external representatives concerning specific operations

Vast knowledge of cGMP’s and direct experience in inspections conducted by various regulatory inspection agencies such as EMEA and FDA

Manage process changes to support overall cGMP compliance.

Fulfill other job duties that may be assigned from time to time

At least 6 years of experience supervising employees in a Biotech manufacturing environment

Maintain current knowledge of the GxPs and optimize GSK’s Quality Management System (QMS)

Audit/inspection e.g., inspection preparation / management / response, on-going inspection readiness

Lead, manage, coach, mentor, retain, and develop staff

Proactively identify continuous improvement opportunities and deliver both improvements and benefits

Or Master’s degree and at least 6+ years of previous pharmaceuticals industry experience in manufacturing, technical, and/or quality role(s).

3+ years of sterile/aseptic drug product manufacturing experience

Possess professional experience working in commercial functions such as Sales, Business Development, and Key Account Management

Ensure exceptional client experience across all touchpoints by effectively leading the Commercial team

Have experience in leading and managing commercial teams

Exhibit strong networking skills and ability to establish connections with people from diverse backgrounds

Possess exceptional verbal and written communication skills

Exhibit independent critical thinking and creative problem-solving skills

Skilled in working collaboratively with Senior Management teams, as well as Partners and other key decision makers within the industry

Oversee the preparation and management of complex GMP manufacturing facility development plans, budgets, and long-range planning

Strong experience in product/process development and/or commercial manufacturing experience in the pharmaceutical industry

Demonstrated experience in senior leadership roles

Brings extensive industry experience and established network within industry

VP of Commercial Operations - Responsibilities

Possess several years of experience in Sales or Business Development

Demonstrate strong communication skills, both written and verbal

VP of Business Development - Responsibilities:

VP of Business Development - Requirements:

Establish, develop, and close business deals

Direct outreach initiatives to potential partners, evaluate opportunities and negotiate contract terms

Support life cycle management of deployed ML apps (e.g., new releases, change management, monitoring and troubleshooting).

Experience on working within compliance (e.g.: quality, regulatory - data privacy, GxP, SOX) and cybersecurity requirements is a plus.

Leading Edge Tech Stack: Experience build products that will be deployed globally on a leading-edge tech stack.

World Class Mentorship and Training: Working with renowned, published leaders and academics in machine learning to further develop your skillsets.

5+ years of experience as a MLOps or ML Engineer, preferably building and maintaining machine learning models.

2+ years of experience deploying and monitoring ML applications at scale across a range of models and platforms.

Organizational management and experience building lean and agile teams

Bachelor of Science (BS) Degree in life sciences or equivalent with fifteen (15) years of relevant experience

Master of Science (MS) Degree in life sciences or equivalent with twelve (12) years of relevant experience

PhD in life sciences or equivalent with ten (10) years of relevant experience

In-depth knowledge of financial systems (budgets, expenses, product standards and variances)

Build diverse talent with the capabilities necessary for future success.

Provide regular updates to management;

Excellent leadership, organizational and managerial skills

Experience in formulation and characterization of parenteral drug delivery systems;

Experience with developability assessment of polymer-drug to support early CMC development

Knowledgeable in design-of-experiments (DOE) and quality-based-design (QbD)

At least 5 years of relevant experience in cGMP drug manufacturing