Perform all activities in compliance with Osmotica Quality System, site environmental, health and safety rules; and applicable FDA and international regulations. * Maintain knowledge of current ...
Perform all activities in compliance with Osmotica Quality System, site environmental, health and safety rules; and applicable FDA and international regulations. * Maintain knowledge of current ...
Description The Analytical Chemist is responsible for testing raw materials, in-process materials, and finished products to support release and stability programs. Essential Responsibilities:
Description The Analytical Chemist is responsible for testing raw materials, in-process materials, and finished products to support release and stability programs. Essential Responsibilities:
POSITION OVERVIEW Conduct and write formal investigation of process deviations for Manufacturing with the assistance of site personnel. This position will also perform initial and final impact risk ...
POSITION OVERVIEW Conduct and write formal investigation of process deviations for Manufacturing with the assistance of site personnel. This position will also perform initial and final impact risk ...
Description Manages all manufacturing and related activities required to support the production of clinical supplies, commercial batches, development, engineering and registration batches of oral ...
Description Manages all manufacturing and related activities required to support the production of clinical supplies, commercial batches, development, engineering and registration batches of oral ...
Associate Director of Manufacturing Operations
Marietta, GA · On-site
$90 - $130/hr
Description Manages all manufacturing and related activities required to support the production of clinical supplies, commercial batches, development, engineering and registration batches of oral ...
New
Associate Director of Manufacturing Operations
Marietta, GA · On-site
$90 - $130/hr
Description Manages all manufacturing and related activities required to support the production of clinical supplies, commercial batches, development, engineering and registration batches of oral ...
New
Osmotica information
What are some common challenges faced by pharmaceutical sales representatives at Osmotica, and how can new hires prepare for them?
Pharmaceutical sales representatives at Osmotica often encounter challenges such as staying up-to-date with complex product information, building trust with healthcare professionals, and navigating regulatory guidelines. New hires can prepare by thoroughly studying product literature, participating in ongoing training, and developing strong communication skills. Additionally, shadowing experienced team members and actively seeking feedback can help new representatives adapt quickly and excel in the fast-paced environment.
What are the key skills and qualifications needed to thrive as an Osmotica pharmaceutical sales representative, and why are they important?
To thrive as a pharmaceutical sales representative at Osmotica, you generally need a bachelor’s degree in life sciences or business, strong knowledge of medical terminology, and sales experience. Familiarity with CRM software, data analysis tools, and compliance with industry regulations like HIPAA is typically required. Outstanding interpersonal communication, persuasive negotiation, and resilience are crucial soft skills for building relationships with healthcare professionals. These competencies ensure that representatives can effectively promote products, maintain compliance, and achieve sales targets in a competitive healthcare market.
What is an osmotica?
An osmotica is a substance used to create or maintain osmotic pressure in a solution, often in biological or pharmaceutical contexts. In plant physiology, osmotica help maintain cell turgor by regulating water movement, while in drug delivery, they can control the release rate of medications in osmotic-controlled oral delivery systems. The choice and concentration of osmotica are critical for ensuring the desired physiological or therapeutic effect.
What is the difference between Osmotica vs Pharmacist?
| Aspect | Osmotica | Pharmacist |
|---|---|---|
| Required Credentials | Typically requires a degree in pharmaceutical sciences or related field | Requires a Doctor of Pharmacy (PharmD) degree and licensure |
| Work Environment | Research labs, pharmaceutical companies, or clinical settings | Community pharmacies, hospitals, or clinics |
| Industry Usage | Pharmaceutical development and research | Dispensing medications and patient counseling |
Osmotica generally refers to a pharmaceutical company involved in drug development, whereas a Pharmacist is a healthcare professional who dispenses medications. While both are connected to the pharmaceutical industry, Osmotica focuses on research and product creation, and Pharmacists focus on patient care and medication management.
More about Osmotica jobs
What cities are hiring for Osmotica jobs? Cities with the most Osmotica job openings:
What states have the most Osmotica jobs? States with the most job openings for Osmotica jobs include:
What job categories do people searching Osmotica jobs look for? The top searched job categories for Osmotica jobs are:
Full-time
Re-posted 27 days ago
Job description
Position Overview
The Quality Inspector is primarily responsible for supporting activities on the production floor. This includes room release, line clearance, in-process batch record review or post-executed review to ensure proper good documentation practices are followed. Provide quality oversight to all production areas to ensure product quality and compliance to cGMPs. This person works closely with operations personnel ensuring cGMP concerns are identified and resolved appropriately. Must be available/flexible to work second or third shift and weekends.
Duties and Responsibilities
- Required to be on-the-floor and present to provide quality oversight for all critical manufacturing and packaging processes.
- Perform QA release and line clearance inspections, AQL checks on product.
- Perform Label Control functions (issuance and reconciliation).
- Perform testing of incoming printed labeling materials
- Conduct review of batch records.
- Perform sampling of the Purified Water System
- Identify deviations and ensure investigations are initiated by the appropriate personnel.
- Clearly communicate complex issues to Management personnel.
- Support creation / revision of SOPs to reflect current practices.
- Assist with FDA and other regulatory inspections.
- Perform all activities in compliance with Osmotica Quality System, site environmental, health and safety rules; and applicable FDA and international regulations.
- Maintain knowledge of current regulatory requirements pertaining to drug product manufacture.
- Perform additional duties and responsibilities as assigned.
Core Competencies
- Position requires the ability to work independently and effectively in all areas of communication, collaboration, and decision-making.
- Great attention to detail with ability to work on multiple projects.
- Ability to organize and adapt to organization priority changes and work effectively with minimal supervision / independently with a sense of urgency.
- Collaborate with Production, Warehouse and other QA team members as partners.
- Computer experience required; Proficiency in Microsoft Office (Word, Excel).
Experience and Qualifications
- High School Diploma or equivalent or technical school certificate.
- Two years of experience in, or support of, pharmaceutical or biotech GMP manufacturing.
- Proficient knowledge of a GMP production facility, manufacturing processes, and/or inspection processes.
- Demonstrated understanding and application of cGMP, current industries practices and relevant guidance.
- Excellent written and verbal communication skills.
- Ability to multi-task effectively.
- Quality Assurance experience a plus.