Scientist - Development

Full Time
Wilmington, NC 28405
Posted
Job description

Are you an experienced Scientist looking for more growth and opportunity to impact lives? Do you have an analytical background or recently graduated with a degree in pharmaceutical sciences and a passion for lab work? If so Alcami is looking for you! Apply Today!

Position Summary

The Scientist is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. A Scientist will routinely lead method development/method validation projects. For this position, HPLC, dissolution and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include: CKF/KF, ICP-MS, Particle Size, CCIT, UV. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile.

Essential Functions

  • Combination of basic and advanced skills in multiple techniques: residual solvents, assays (potencies, related substances), dissolution, elemental impurities, moisture content, identification, and other various analytical techniques.
  • Achieves results by solving problems of a diverse scope.
  • Drives initiatives outside of standard work function.
  • Writes methods, test procedures, protocols and reports.
  • Strong equipment troubleshooting skills.
  • Leads investigations and root cause analysis.
  • Executes method development/validation and routine testing with little to no assistance.
  • Maintains working knowledge of routine instrumentation, equipment, and scientific methodologies necessary to perform assigned tasks.
  • Performs assigned tasks carefully and on schedule according to standard operating procedure and supervisor instructions.
  • Analyzes information for technical correctness and accuracy.
  • Complies with applicable GMPs, peer checks information and signs for GMP review. Brings aberrant information to the attention of supervisor.
  • Participates in company sponsored training and maintains current status of certifications.
  • Maintains a safe, clean, and organized work environment free of safety hazards.
  • Suggests improvements for safety, work quality, and productivity.
  • Ensures timely completion and compliance with cGMP and all other relevant company training requirements
  • Discuss and review critical testing results with clients.
  • Seeks to cultivate mentorship, build leadership skills and foster a culture of “Team First”

Education and Experience

  • Bachelor’s degree in Chemistry or a related field with with 8-10 years industry experience or a Master’s degree with 5-7 years of experience required.
  • Prior laboratory experience or work experience in pharmacuetical, CDMO or cGMP preferred.

Alcami Non-Negotiables

  • Consistently demonstrates honesty and integrity through personal example.
  • Follows all safety policies and leads by example a safety first culture.
  • Produces high quality work product with a focus on first time right.
  • Complies with the company code of conduct and policies and regulatory standards.

Alcami Core Leadership Competencies

  • Thinks strategically. Quickly identifies and acts on opportunities. Considers the downstream impact. Seeks to understand the why. Focuses on work that matters.
  • Develops organization and others. Takes ownership to develop self and others. Seeks out new opportunities and experiences for continuous learning.
  • Acts decisively. Makes and acts on decisions quickly. Makes decisions with the customer and their patients in mind. Meets commitments with a sense of urgency. Seeks ways to be more efficient.
  • Drives performance. Holds self and others accountable. Delivers results first time right. Never settles for status quo. Willing to have tough conversations. Asks for feedback and takes action to improve.
  • Passion for customers. Listens to understand. Asks the right questions. Gets to the heart of the matter and uses that insight to provide value.
  • Works collaboratively. Seeks out the experience of others with the aim for better results. Open minded regardless where ideas originate. Flexible and easy to work with.

Functional Competencies

  • Excellent verbal and written communication and documentation skills required.
  • Excellent detail orientation and organizational skills required.
  • Excellent problem-solving and basic trouble-shooting ability required.
  • Excellent knowledge of Laboratory equipment and safety required.
  • Excellent knowledge of Laboratory Documentation is required.
  • Strong knowledge of cGMP in a pharmaceutical or regulated environment preferred.
  • Proficiency with Microsoft Office (Word, Excel, PowerPoint) required.

Decision Making and Supervision Required

  • Applies job skills, company policies and SOPs to complete a variety of tasks.
  • Receives general instructions on routine work, detailed instructions on new projects or assignments.

Travel Requirements

  • Up to 5% travel required.

Job Type: Full-time

Pay: $68,000.00 - $80,000.00 per year

Benefits:

  • 401(k)
  • 401(k) matching
  • Dental insurance
  • Employee assistance program
  • Employee discount
  • Flexible schedule
  • Flexible spending account
  • Health insurance
  • Health savings account
  • Life insurance
  • Paid time off
  • Parental leave
  • Professional development assistance
  • Referral program
  • Relocation assistance
  • Tuition reimbursement
  • Vision insurance

Schedule:

  • 8 hour shift
  • Day shift
  • Monday to Friday
  • Overtime

Supplemental pay types:

  • Bonus pay

Experience:

  • Laboratory experience: 5 years (Required)

Work Location: One location

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